Edgard da Veiga Lion Neto is a clinical researcher and medical manager with over 25 years of experience in the pharmaceutical industry. He has worked with many major pharmaceutical companies, including Novartis, Sanofi, Boehringer Ingelheim, and Pfizer. His experience includes managing clinical trials, developing marketing strategies, training sales teams, and providing scientific and regulatory support. He has advanced degrees in medicine, business administration, and legal medicine.
Dr. Andrea Csobó's curriculum vitae provides information about her personal details, education, employment history, skills, languages, and hobbies. She has over 25 years of experience in the pharmaceutical industry, holding roles such as sales representative, regional sales manager, key account manager, and medical science liaison. Her employment history details her responsibilities and achievements in each role with Company 2, 3, and 4, notably Novartis Pharma Ltd from 1998-2014. She has strong communication, leadership, and medical knowledge.
Alexandr Mészáros has over 20 years of experience in pharmacovigilance and clinical research. He currently works as an independent pharmacovigilance consultant in Switzerland, providing quality oversight and compliance training. Previously, he held roles such as Drug Safety Physician and Senior Manager Pharmacovigilance at Acino Pharma AG and BASILEA Pharmaceutica International Ltd in Switzerland, where he established and optimized pharmacovigilance systems. He also has experience as a Clinical Research Associate and Site Developer for global clinical research organizations. Mészáros received his medical degree from Uzhgorod State University in Ukraine and completed post-graduate studies in pharmacoepidemiology from the University of
Michael Kalpaxoglou has over 25 years of experience in healthcare market research and the pharmaceutical industry. He is currently the Healthcare Research Director at Ipsos Opinion, a market research company in Greece. Prior to this role, he held several managerial positions at other pharmaceutical companies, including District Manager and Sales & Marketing Effectiveness Senior Manager at Amgen Hellas. He has extensive expertise in areas such as oncology, infectious diseases, and healthcare policies and reforms.
VERSA PULS MEDIA, associate of VERSA MEDIA international publishing group since 2008, is a Romanian leading communication company providing specialized information to the medical community for continuous professional development, and to consumers for adopting a healthy lifestyle. VERSA PULS MEDIA delivers high-quality promotion solutions to companies that offer products and services for better health.
Puls Media Network is a leading Romanian communication company specialized in the medical field. It publishes 8 specialized medical journals reaching over 30,000 medical professionals. It also publishes an annual consumer health publication with a circulation of 30,000. Additionally, it organizes over 50 medical events per year and operates a medical information portal. Puls Media Network aims to provide specialized information to medical professionals and consumers to support continuous learning and healthy lifestyles.
Targos Molecular Pathology GmbH and WuXi PharmaTech announced a strategic collaboration to provide clinical biomarker services and pathology training in China. Through this collaboration, Targos will provide expertise, services, and quality standards to support WuXi's work in biomarkers for cancer patients. Targos will also provide internationally recognized training to local pathologists and histotechnologists. This agreement allows WuXi to offer a comprehensive platform of soluble, cell, and tissue biomarker services to customers.
Samantha Gross is a registered pharmacist in Massachusetts with 7 years of experience in biotech and pharmaceutical science. She has a Doctor of Pharmacy degree from MCPHS University and a Bachelor's degree in Environmental Biology from Unity College. Her experience includes positions at Biogen, CVS Caremark, Novartis, and several hospitals. She has expertise in delivering quality customer service, proficiency in Microsoft Office, and regulatory affairs experience from her internship at Biogen.
Dr. Andrea Csobó's curriculum vitae provides information about her personal details, education, employment history, skills, languages, and hobbies. She has over 25 years of experience in the pharmaceutical industry, holding roles such as sales representative, regional sales manager, key account manager, and medical science liaison. Her employment history details her responsibilities and achievements in each role with Company 2, 3, and 4, notably Novartis Pharma Ltd from 1998-2014. She has strong communication, leadership, and medical knowledge.
Alexandr Mészáros has over 20 years of experience in pharmacovigilance and clinical research. He currently works as an independent pharmacovigilance consultant in Switzerland, providing quality oversight and compliance training. Previously, he held roles such as Drug Safety Physician and Senior Manager Pharmacovigilance at Acino Pharma AG and BASILEA Pharmaceutica International Ltd in Switzerland, where he established and optimized pharmacovigilance systems. He also has experience as a Clinical Research Associate and Site Developer for global clinical research organizations. Mészáros received his medical degree from Uzhgorod State University in Ukraine and completed post-graduate studies in pharmacoepidemiology from the University of
Michael Kalpaxoglou has over 25 years of experience in healthcare market research and the pharmaceutical industry. He is currently the Healthcare Research Director at Ipsos Opinion, a market research company in Greece. Prior to this role, he held several managerial positions at other pharmaceutical companies, including District Manager and Sales & Marketing Effectiveness Senior Manager at Amgen Hellas. He has extensive expertise in areas such as oncology, infectious diseases, and healthcare policies and reforms.
VERSA PULS MEDIA, associate of VERSA MEDIA international publishing group since 2008, is a Romanian leading communication company providing specialized information to the medical community for continuous professional development, and to consumers for adopting a healthy lifestyle. VERSA PULS MEDIA delivers high-quality promotion solutions to companies that offer products and services for better health.
Puls Media Network is a leading Romanian communication company specialized in the medical field. It publishes 8 specialized medical journals reaching over 30,000 medical professionals. It also publishes an annual consumer health publication with a circulation of 30,000. Additionally, it organizes over 50 medical events per year and operates a medical information portal. Puls Media Network aims to provide specialized information to medical professionals and consumers to support continuous learning and healthy lifestyles.
Targos Molecular Pathology GmbH and WuXi PharmaTech announced a strategic collaboration to provide clinical biomarker services and pathology training in China. Through this collaboration, Targos will provide expertise, services, and quality standards to support WuXi's work in biomarkers for cancer patients. Targos will also provide internationally recognized training to local pathologists and histotechnologists. This agreement allows WuXi to offer a comprehensive platform of soluble, cell, and tissue biomarker services to customers.
Samantha Gross is a registered pharmacist in Massachusetts with 7 years of experience in biotech and pharmaceutical science. She has a Doctor of Pharmacy degree from MCPHS University and a Bachelor's degree in Environmental Biology from Unity College. Her experience includes positions at Biogen, CVS Caremark, Novartis, and several hospitals. She has expertise in delivering quality customer service, proficiency in Microsoft Office, and regulatory affairs experience from her internship at Biogen.
Clinical Trial Registries: Panacea or Pablum?Michael Swit
Clinical trial registries have evolved to increase transparency of clinical research. The 2007 FDA Amendments Act (FDAAA) expanded requirements for registration and disclosure of trial information and results. FDAAA requires registration of most clinical trials of drugs and devices and posting of basic results data and links to FDA submissions. It aims to help patients find trials and allow evaluation of evidence but registries face challenges regarding premature disclosure, data interpretation and patient/physician burden.
Companyprofilesandconferences.com glad to promote a new report on "Diaxonhit S.A (ALEHT) - Product Pipeline Analysis" which is a source for data, analysis, and actionable intelligence on the company’s portfolio of pipeline products who provides key information about the company, its major products and brands.
Professional relations and practices of hospital pharmacisvikasaagrahari007
This document discusses the professional relationships and practices of hospital pharmacists. It begins by defining a hospital pharmacy as a pharmacy or department within a hospital managed by a qualified pharmacist. It then describes the roles of hospital pharmacists, which include preparing and dispensing medications, educating patients, monitoring drug interactions, and administering the pharmacy department. The document goes on to discuss how hospital pharmacists can promote their profession through maintaining relationships with other medical professionals, patients, and the pharmaceutical industry. It also outlines some of the key practices of hospital pharmacists, such as participating in teaching, organizing educational services for the public, and participating in professional associations.
Hospital pharmacy involves the supervision of medications by a pharmacist. It forecasts demand, selects suppliers, manufactures sterile and non-sterile preparations, conducts quality control, dispenses medications to patients and outpatients, provides drug information, studies drug utilization, implements pharmacy committee recommendations, counsels patients, and maintains liaison between medical, nursing and patient staff. It is responsible for staffing, storage, distribution of drugs, and addressing problems while minimizing carrying costs of inventory.
A hospital staff pharmacist provides pharmacy services to both inpatients and outpatients at a hospital. They work closely with doctors and nurses to administer medications to patients and may prepare specialized medications. Hospital pharmacists are experts in medications and work to ensure patients receive the best treatment. Key responsibilities include dispensing prescriptions accurately, advising medical staff on drug selection and dosage, and educating patients. A degree in pharmacy is required to become a licensed hospital pharmacist.
The document outlines ASHP's position that pharmacy departments should provide emergency departments with necessary pharmacy services to ensure safe and effective patient care. It recommends pharmacists work with ED staff on medication safety initiatives and provide clinical services like reviewing orders and reconciling medications. The document discusses evidence that pharmacist involvement in EDs can reduce medication errors and adverse drug events. It provides examples of pharmacy roles in areas like emergency preparedness, quality improvement, education, and research. Finally, it calls for expanding pharmacy education and training opportunities in emergency care.
Tony Lockett has over 25 years of experience in the pharmaceutical and medical devices industry. He has acted as a consultant advising clients on regulatory and clinical strategies, and has also acted as Chief Medical Officer for an AIM-listed company. Currently, through his company, he is co-developing re-positioned and re-profiled medical products.
Monishankar Saha has over 15 years of experience in drug regulatory affairs and business development. He is currently the Manager of Drug Regulatory Affairs at Novartis Bangladesh, where he leads regulatory compliance projects and ensures global regulatory standards are met. Prior to this role, he gained experience in quality control, business development, and regulatory affairs at other pharmaceutical companies. He has extensive training in global regulatory strategies and maintains relationships with regulatory stakeholders.
This document is a resume for Elaine G. Warner, JD, MS, RN. It summarizes her education, which includes degrees in nursing, early childhood education, and law. It also outlines her extensive work experience in nursing, medical science liaison roles, consulting, and teaching. She has over 30 years of experience in healthcare.
Dr. Syed Javaid Khurshid has over 37 years of experience working for the Pakistan Atomic Energy Commission, where he currently serves as the Director of Projects Coordination and Chairman Secretariat. He has a PhD in bioinorganic chemistry and has extensive experience managing projects in areas like agriculture, biotechnology, energy, engineering, and medicine totaling over $1.2 billion. Dr. Khurshid also teaches at several universities and has over 50 publications in international and national journals.
Fernando Marchán is a highly accomplished pharmaceutical sales and marketing executive with over 25 years of experience leading top performing teams. He has a proven track record of developing strategic plans that drive outstanding financial results, including being named a President's Circle Winner and leading multiple districts and regions to #1 rankings nationally. Marchán has expertise across many therapeutic areas and excels at developing talent within sales organizations.
This document provides biographical and employment details for Dr. GUNARETNAM RAJAGOPAL. It outlines his current role as Global Head of Computational Sciences at Janssen Pharma R&D and lists his previous employment history. It also provides details of his education background and areas of expertise including total informatics strategy, integrative genomics, translational informatics, computational/systems biology, and cyber-infrastructure development. Finally, it describes some of his current and previous research projects focused on drug discovery, big data analytics, and collaborations with academic and industry partners.
Suparna Paruthy is a computer science student at USC seeking job opportunities. She has a Master's in Computer Science from USC with a 3.37 GPA and a Bachelor's in Computer Science Engineering from Mody Institute of Technology & Science with an 8.74 CGPA. She has skills in languages like C, C++, Java, and PHP and tools like Visual Studio, Eclipse, and MS Office. She has work experience as a software engineer at Accenture and internships at i3indya Technologies and NIC. Her projects include a search engine for Keck School of Medicine, real estate websites and apps using Zillow API, and an embedded smart home system.
Thomas Graves is a full stack web developer based in New York City. He has experience developing web applications using technologies like HTML, CSS, JavaScript, React, Ruby on Rails, and Python. His most recent projects include FrienDiagram, a platform for finding equidistant venues for friends using Google Maps API, and SetState(), a recreation of the game Set using React and algorithms to determine card matches. Graves has a business administration degree and experience teaching English abroad in South Korea.
This document is a resume for Gaël PORTÉ, an embedded software engineer with experience developing middleware and applications using C++, Qt, and other technologies. Some key details:
- Gaël has 4 years of experience developing middleware and software using C++ and Qt, including projects involving payment devices, medical monitoring applications, and more.
- Previous roles include embedded software engineer positions at Witekio and eROCCA developing applications on ARM boards using C/C++ and Qt.
- Gaël has also worked as an intern developing tools for automotive powertrain analysis and a web developer internship involving telescope databases.
- Education includes a Master's degree in Computer Science and
Laurent Hennequin has over 30 years of experience in field application engineering and product management roles. Most recently, he was a Product Manager and Sales Engineer for TOKHATEC in France from 2013 to 2016, managing supplier relationships and growing customer portfolio. Prior to that, he spent 13 years as a Senior Field Application Engineer at Intel Corporation, providing technical support and managing accounts in France, Iberia, Benelux, and Japan. He has a background in hardware development, having worked at SAGEM from 1983 to 1990.
The document provides a summary of qualifications for a Brazil Market Place: Commercial Director / Sales Manager / Sales Consultant position. It outlines over 22 years of experience in sales and management for industrial lubricants and metalworking fluids, with expertise in sectors like automotive, food processing, aerospace, and manufacturing. Responsibilities have included developing sales strategies, reorganizing teams, implementing processes to improve profitability and efficiency, and maintaining strong customer relationships. Educational background includes an engineering degree and additional training in areas like leadership, accounting, and metalworking technologies.
This document contains a professional summary for Akanksha Sharma. She has 3.6 years of experience as a Software Engineering Analyst working on system development and integration of enterprise applications using Oracle SOA Suite. Her skills include Oracle Fusion Middleware technologies, SOA implementations using web services, and working with tools like JDeveloper and Oracle WebLogic Server. She has worked on projects for telecommunications clients, building interfaces between systems using technologies like BPEL, Oracle Service Bus, and customizing Oracle applications. Akanksha has a Bachelor's degree in Computer Engineering and diploma in Computer Science.
The candidate is a full-stack web developer who is passionate about using their creative abilities to build apps and websites. They have experience in security management roles where they maintained security systems, investigated criminal activity, and organized system overhauls. The candidate also completed a full-stack web development course at Bitmaker Labs and has skills in Ruby on Rails, JavaScript, HTML5, CSS3, Unix, and Git.
Clinical Trial Registries: Panacea or Pablum?Michael Swit
Clinical trial registries have evolved to increase transparency of clinical research. The 2007 FDA Amendments Act (FDAAA) expanded requirements for registration and disclosure of trial information and results. FDAAA requires registration of most clinical trials of drugs and devices and posting of basic results data and links to FDA submissions. It aims to help patients find trials and allow evaluation of evidence but registries face challenges regarding premature disclosure, data interpretation and patient/physician burden.
Companyprofilesandconferences.com glad to promote a new report on "Diaxonhit S.A (ALEHT) - Product Pipeline Analysis" which is a source for data, analysis, and actionable intelligence on the company’s portfolio of pipeline products who provides key information about the company, its major products and brands.
Professional relations and practices of hospital pharmacisvikasaagrahari007
This document discusses the professional relationships and practices of hospital pharmacists. It begins by defining a hospital pharmacy as a pharmacy or department within a hospital managed by a qualified pharmacist. It then describes the roles of hospital pharmacists, which include preparing and dispensing medications, educating patients, monitoring drug interactions, and administering the pharmacy department. The document goes on to discuss how hospital pharmacists can promote their profession through maintaining relationships with other medical professionals, patients, and the pharmaceutical industry. It also outlines some of the key practices of hospital pharmacists, such as participating in teaching, organizing educational services for the public, and participating in professional associations.
Hospital pharmacy involves the supervision of medications by a pharmacist. It forecasts demand, selects suppliers, manufactures sterile and non-sterile preparations, conducts quality control, dispenses medications to patients and outpatients, provides drug information, studies drug utilization, implements pharmacy committee recommendations, counsels patients, and maintains liaison between medical, nursing and patient staff. It is responsible for staffing, storage, distribution of drugs, and addressing problems while minimizing carrying costs of inventory.
A hospital staff pharmacist provides pharmacy services to both inpatients and outpatients at a hospital. They work closely with doctors and nurses to administer medications to patients and may prepare specialized medications. Hospital pharmacists are experts in medications and work to ensure patients receive the best treatment. Key responsibilities include dispensing prescriptions accurately, advising medical staff on drug selection and dosage, and educating patients. A degree in pharmacy is required to become a licensed hospital pharmacist.
The document outlines ASHP's position that pharmacy departments should provide emergency departments with necessary pharmacy services to ensure safe and effective patient care. It recommends pharmacists work with ED staff on medication safety initiatives and provide clinical services like reviewing orders and reconciling medications. The document discusses evidence that pharmacist involvement in EDs can reduce medication errors and adverse drug events. It provides examples of pharmacy roles in areas like emergency preparedness, quality improvement, education, and research. Finally, it calls for expanding pharmacy education and training opportunities in emergency care.
Tony Lockett has over 25 years of experience in the pharmaceutical and medical devices industry. He has acted as a consultant advising clients on regulatory and clinical strategies, and has also acted as Chief Medical Officer for an AIM-listed company. Currently, through his company, he is co-developing re-positioned and re-profiled medical products.
Monishankar Saha has over 15 years of experience in drug regulatory affairs and business development. He is currently the Manager of Drug Regulatory Affairs at Novartis Bangladesh, where he leads regulatory compliance projects and ensures global regulatory standards are met. Prior to this role, he gained experience in quality control, business development, and regulatory affairs at other pharmaceutical companies. He has extensive training in global regulatory strategies and maintains relationships with regulatory stakeholders.
This document is a resume for Elaine G. Warner, JD, MS, RN. It summarizes her education, which includes degrees in nursing, early childhood education, and law. It also outlines her extensive work experience in nursing, medical science liaison roles, consulting, and teaching. She has over 30 years of experience in healthcare.
Dr. Syed Javaid Khurshid has over 37 years of experience working for the Pakistan Atomic Energy Commission, where he currently serves as the Director of Projects Coordination and Chairman Secretariat. He has a PhD in bioinorganic chemistry and has extensive experience managing projects in areas like agriculture, biotechnology, energy, engineering, and medicine totaling over $1.2 billion. Dr. Khurshid also teaches at several universities and has over 50 publications in international and national journals.
Fernando Marchán is a highly accomplished pharmaceutical sales and marketing executive with over 25 years of experience leading top performing teams. He has a proven track record of developing strategic plans that drive outstanding financial results, including being named a President's Circle Winner and leading multiple districts and regions to #1 rankings nationally. Marchán has expertise across many therapeutic areas and excels at developing talent within sales organizations.
This document provides biographical and employment details for Dr. GUNARETNAM RAJAGOPAL. It outlines his current role as Global Head of Computational Sciences at Janssen Pharma R&D and lists his previous employment history. It also provides details of his education background and areas of expertise including total informatics strategy, integrative genomics, translational informatics, computational/systems biology, and cyber-infrastructure development. Finally, it describes some of his current and previous research projects focused on drug discovery, big data analytics, and collaborations with academic and industry partners.
Suparna Paruthy is a computer science student at USC seeking job opportunities. She has a Master's in Computer Science from USC with a 3.37 GPA and a Bachelor's in Computer Science Engineering from Mody Institute of Technology & Science with an 8.74 CGPA. She has skills in languages like C, C++, Java, and PHP and tools like Visual Studio, Eclipse, and MS Office. She has work experience as a software engineer at Accenture and internships at i3indya Technologies and NIC. Her projects include a search engine for Keck School of Medicine, real estate websites and apps using Zillow API, and an embedded smart home system.
Thomas Graves is a full stack web developer based in New York City. He has experience developing web applications using technologies like HTML, CSS, JavaScript, React, Ruby on Rails, and Python. His most recent projects include FrienDiagram, a platform for finding equidistant venues for friends using Google Maps API, and SetState(), a recreation of the game Set using React and algorithms to determine card matches. Graves has a business administration degree and experience teaching English abroad in South Korea.
This document is a resume for Gaël PORTÉ, an embedded software engineer with experience developing middleware and applications using C++, Qt, and other technologies. Some key details:
- Gaël has 4 years of experience developing middleware and software using C++ and Qt, including projects involving payment devices, medical monitoring applications, and more.
- Previous roles include embedded software engineer positions at Witekio and eROCCA developing applications on ARM boards using C/C++ and Qt.
- Gaël has also worked as an intern developing tools for automotive powertrain analysis and a web developer internship involving telescope databases.
- Education includes a Master's degree in Computer Science and
Laurent Hennequin has over 30 years of experience in field application engineering and product management roles. Most recently, he was a Product Manager and Sales Engineer for TOKHATEC in France from 2013 to 2016, managing supplier relationships and growing customer portfolio. Prior to that, he spent 13 years as a Senior Field Application Engineer at Intel Corporation, providing technical support and managing accounts in France, Iberia, Benelux, and Japan. He has a background in hardware development, having worked at SAGEM from 1983 to 1990.
The document provides a summary of qualifications for a Brazil Market Place: Commercial Director / Sales Manager / Sales Consultant position. It outlines over 22 years of experience in sales and management for industrial lubricants and metalworking fluids, with expertise in sectors like automotive, food processing, aerospace, and manufacturing. Responsibilities have included developing sales strategies, reorganizing teams, implementing processes to improve profitability and efficiency, and maintaining strong customer relationships. Educational background includes an engineering degree and additional training in areas like leadership, accounting, and metalworking technologies.
This document contains a professional summary for Akanksha Sharma. She has 3.6 years of experience as a Software Engineering Analyst working on system development and integration of enterprise applications using Oracle SOA Suite. Her skills include Oracle Fusion Middleware technologies, SOA implementations using web services, and working with tools like JDeveloper and Oracle WebLogic Server. She has worked on projects for telecommunications clients, building interfaces between systems using technologies like BPEL, Oracle Service Bus, and customizing Oracle applications. Akanksha has a Bachelor's degree in Computer Engineering and diploma in Computer Science.
The candidate is a full-stack web developer who is passionate about using their creative abilities to build apps and websites. They have experience in security management roles where they maintained security systems, investigated criminal activity, and organized system overhauls. The candidate also completed a full-stack web development course at Bitmaker Labs and has skills in Ruby on Rails, JavaScript, HTML5, CSS3, Unix, and Git.
Shiping Yan (Mike) is a senior test lead at IBM China Development Labs with over 10 years of experience in software development and testing. He has led and participated in multiple large, complex projects involving geographically distributed teams. Mike has strong skills in communication, team management, understanding business needs, and designing and executing effective tests. He has experience across various product and solution testing areas, and is proficient in languages like Java and C++.
This document contains the resume of Suhail Ahamed, who has over 9 years of experience as a Technical Manager and Senior Software Engineer. He has expertise in various technologies like .NET, SQL Server, JavaScript and has experience building applications for industries like retail, healthcare and ecommerce. Some of the key projects mentioned in the resume are PyXis order management system, Center for Medicare product ordering system and various credit monitoring and identity protection applications for clients like Citi, Chase and First Advantage.
Suzanne Pierce has over 25 years of experience as a clinical nurse in high risk obstetrics and 5 years of experience in telephonic high risk obstetric case management. She holds active nursing licenses in 8 states and has worked in various telephonic case management and clinical nursing roles. Her experience includes providing education to high risk pregnant patients, ensuring culturally competent care, utilization review, and clinical case management. She has strong clinical skills and experience in areas such as prenatal nutrition, breastfeeding education, and high risk antenatal monitoring.
Pieter Van der Vyver is an electronic engineer from South Africa with expertise in computational neuroscience, machine learning, and software engineering. He has a Master's degree in electronic engineering and speaks several languages. He has worked on research projects involving cochlear implants and speech encoding. His professional experience includes positions in research, technical delivery management, and software development using technologies such as IBM Rational, Matlab, and various programming languages. He has received several awards for his work.
This document provides a summary of a middleware developer's experience and qualifications. The developer has over 4 years of experience working with Oracle middleware technologies like SOA, BPEL, ESB, and Mediator. Some of the key projects listed include developing BPEL processes and services for telecom companies in Africa and implementing Oracle SOA, OSB, and BPEL for financial services projects in the US. The developer also has skills in XML, SQL, and administering WebLogic application servers.
Med Knowledge Imp to Sales Team - Role of Med. Aff. Speaker Dr. KK 2023 10 03...AmeetRathod3
This document provides an overview of the importance of medical knowledge for sales and marketing teams in the pharmaceutical industry. It discusses how understanding medical terminology, disease states, and clinical data enhances sales representatives' scientific competency and ability to have effective discussions with physicians. The document also outlines the roles of the medical affairs department in providing training to sales teams on therapy areas, products, clinical trials, and addressing medical queries to improve their knowledge. It emphasizes that physicians prefer engaging with representatives who demonstrate strong clinical and scientific expertise.
TranScrip provides services across the pharmaceutical development lifecycle including translational medicine, clinical development, regulatory affairs, medical affairs, drug safety, and portfolio management. They help biotech and pharmaceutical clients address challenges and achieve their drug development and commercialization goals. Their teams integrate seamlessly with clients and provide expertise, oversight, and flexible support to maximize opportunities and reduce risks throughout the drug development process from early research through commercialization.
Medical affairs department for small organizationDr. Zubair Ali
The document summarizes the drug development process and the role of medical affairs departments within pharmaceutical companies. It discusses the various phases of clinical drug trials from phase I to phase IV. It then outlines the structure and responsibilities of medical affairs, including clinical research, pharmacovigilance, medical information services, statistics management, and providing medical support to marketing and sales teams. A key part of medical affairs is the medical science liaison program which aims to educate medical professionals and support clinical trial recruitment through relationship building.
Tran Chung Thuy is a medical doctor seeking a position in medical affairs, medical science liaison, or product management. He has over 15 years of experience in clinical practice and the pharmaceutical industry, most recently as an MSL at Hoffmann-La Roche promoting hepatitis, anemia, rheumatoid arthritis, and transplantation products. He is proficient in English and Vietnamese and has a strong track record of building relationships with key opinion leaders and external stakeholders.
Career Options for Pharmacists in the Industry (Singapore)yk png
The presentation is intended as an overview for pre-registration pharmacists and newly graduated pharmacists who wish to know the options available for pharmacists in the Industry.
Dina Ahmed Ismail Eldaour seeks a position where she can utilize her skills and experience in medical affairs, compliance, and team leadership. She has over 20 years of experience in medical affairs roles at AstraZeneca, managing medical teams across the Middle East and Africa regions. Her experience includes managing medical information, compliance functions, non-interventional studies, and patient safety. She has strong leadership skills and experience developing medical strategies aligned with organizational objectives.
The Medical Director oversees all activities of a company's Medical Department and contributes to senior leadership. Their day involves emails and phone calls about clinical trials, regulations, and health economics. They attend internal meetings on research, regulations, reimbursement, and business strategies. External meetings include advising investigators and regulators. As the senior medical advisor, they provide clinical guidance across the company.
Square Pharmaceuticals is the largest pharmaceutical company in Bangladesh. It has over 16 departments that handle functions like product management, marketing, finance, HR, and supply chain. Square produces over 400 medicines across various dosage forms like tablets, capsules, injections, liquids and inhalers. External factors affecting the pharmaceutical industry include political pressure on pricing, economic pressures reducing disposable income, an aging population, and increasing regulations.
Vanessa Tasso has over 15 years of experience in healthcare and aerospace operations, specializing in clinical affairs, regulatory compliance, and marketing. She has a proven track record of optimizing business processes, managing clinical trials, gaining regulatory approvals, raising funds, and commercializing new medical technologies. Notable achievements include accelerating patient enrollment in a clinical trial by 500% ahead of schedule and raising $44M for an IPO. She is skilled in developing compliant documentation, navigating international trials, and creating compelling marketing materials to promote new treatments.
Career options for pharmacists in the industryyk png
The document discusses various career options for pharmacists in the pharmaceutical industry in Singapore, including roles in manufacturing, academics, government institutions, hospitals, entrepreneurship, and more. It outlines options such as working in pharmaceutical, consumer healthcare, biotechnology, medical devices, distribution, research and development, clinical trials, sales, product management, regulatory affairs, medical science liaison, quality control and compliance, and training and education. For each role, the document provides examples of job scopes, duties, attributes needed, and advice for pharmacists pursuing careers in the industry. Typical compensation for a pharmaceutical sales representative and the day-to-day work life are also summarized.
Catherine M. Gillis is a healthcare industry consultant with over 25 years of experience conducting market research, strategic planning, and customer insights analysis for companies in various industries including healthcare, biotech, and publishing. She has led strategic planning and market forecasting initiatives for large companies such as Elsevier, Wyeth Vaccines, and Saint-Gobain. Her areas of expertise include market segmentation, competitive intelligence, customer experience research, and developing strategic recommendations based on data analysis. Currently she works as an independent consultant providing customized research for clients in the healthcare field.
Method, tools and recommendations to boost Medical Science Liaisons Competence and performance.
Presentation of best practices to manage key opinion leaders
Views for collaboration between pharmaceutical industry and academia a haapal...Antti Haapalinna
The document discusses views on collaboration between the pharmaceutical industry and academia from Antti Haapalinna, Vice President of Research and Development at Orion Corporation. It notes that strategic partnerships can cover the entire R&D chain from early discovery to late-stage clinical development and marketing. Early-stage partnerships are often with smaller organizations that provide specific expertise to complement larger companies. Later-stage partnerships are usually with larger organizations for their clinical trial expertise and global reach. Key success factors include a mutual desire to develop new treatments, each party contributing unique capabilities, and professionally coordinated collaboration.
Educating KOLs, Physicians, Patients, and Payers to support successful produc...Best Practices, LLC
The document discusses best practices for educating key stakeholders to support successful product launches. It finds that companies should:
1) Start thought leader engagement early, as early as pre-clinical trials, through communication, advisory boards, and developing long-term strategies.
2) Seed medical science liaisons in phase 3 trials and grow their numbers each subsequent year leading up to launch.
3) Oncology companies may be more willing to take risks with investigator-initiated trials earlier to explore new uses and populations.
Greetings from Virtue Insight,
I am happy to invite you and your colleagues to be a sponsor/ delegate for our upcoming “9th Pharmacovigilance 2015” The conference will Be held on 2nd September 2015, Kohinoor Continental Hotel, Mumbai, India. Please find the detailed agenda for the same with this email.
FMD:- + 91 9171350244 or deepak@virtueinsight.co.in, deepakrajvirtueinsight@gmail.com
EUPATI 2013 Conference: Building Knowledge & Competences for Patients’ Involv...EUPATI
EUPATI 2013 Conference: Building Knowledge & Competences for Patients’ Involvement in Medicines R&D, “Bring to life with EUPATI examples”, by Niels Westergaard, PhD, DSc Biopeople, University of Copenhagen, Denmark
£1,000.00
Manager: £1,500.00
Strategic Consultant
£1,500.00
Medical Consultant
£1,500.00
Legal Consultant
£1,500.00
Communication Consultant
£1,500.00
Project Manager
£1,000.00
Administrative Support
£500.00
08/02/2014 confidential
35
Our Costing Procedure
1. Initial meeting to understand the need
2. Proposal of the appropriate level of advice
3. Estimate of required time and team
4. Costing based on our grid
5.
Bill Hatfield is a biotechnology executive with over 20 years of experience in oncology leadership, commercial development, and marketing. He has led the commercial development and US launches of 10 oncology products, including Velcade at Millennium Pharmaceuticals where he achieved $100 million in sales in the first year. Currently he is Senior Vice President of Commercial Development at Karyopharm Therapeutics, leading the commercialization of Selinexor as a potential therapy for hematological malignancies and solid tumors.
M&A activity in 2014 was dynamic, with more in vitro diagnostics (IVD) transactions compared to the previous two years combined. For 2015 to date, Worldwide IVD transactions (including instrument/reagent manufacturers, genome informatics and reference labs) are on par with 2014 activity although there has been a sharp decline in acquisitions in China. Also, EY’s Medtech Firepower Index shows steady growth in “firepower” – which EY defines as a company’s ability to do M&A based on the strength of its balance sheet -- since 2011, indicating high borrowing capacity and the potential for future transaction execution. In particular, the diagnostics market has seen an emergence of creative deal making between nontraditional partners specifically within oncology, NIPT and MRSA.
Whether the interest is developing a new product claim, or there's the need to understand the potential effect of products use and consumption in targeted customers, res4Q is the right choice to ease the pathway and get sound data.
res4Q can identify the right methods and lead your steps towards the right direction, assisting and implementing an ad-hoc research, in order to quickly and professionally answer your necessities.
Osteoporosis - Definition , Evaluation and Management .pdfJim Jacob Roy
Osteoporosis is an increasing cause of morbidity among the elderly.
In this document , a brief outline of osteoporosis is given , including the risk factors of osteoporosis fractures , the indications for testing bone mineral density and the management of osteoporosis
Adhd Medication Shortage Uk - trinexpharmacy.comreignlana06
The UK is currently facing a Adhd Medication Shortage Uk, which has left many patients and their families grappling with uncertainty and frustration. ADHD, or Attention Deficit Hyperactivity Disorder, is a chronic condition that requires consistent medication to manage effectively. This shortage has highlighted the critical role these medications play in the daily lives of those affected by ADHD. Contact : +1 (747) 209 – 3649 E-mail : sales@trinexpharmacy.com
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Kat...rightmanforbloodline
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
share - Lions, tigers, AI and health misinformation, oh my!.pptxTina Purnat
• Pitfalls and pivots needed to use AI effectively in public health
• Evidence-based strategies to address health misinformation effectively
• Building trust with communities online and offline
• Equipping health professionals to address questions, concerns and health misinformation
• Assessing risk and mitigating harm from adverse health narratives in communities, health workforce and health system
Local Advanced Lung Cancer: Artificial Intelligence, Synergetics, Complex Sys...Oleg Kshivets
Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
Histololgy of Female Reproductive System.pptxAyeshaZaid1
Dive into an in-depth exploration of the histological structure of female reproductive system with this comprehensive lecture. Presented by Dr. Ayesha Irfan, Assistant Professor of Anatomy, this presentation covers the Gross anatomy and functional histology of the female reproductive organs. Ideal for students, educators, and anyone interested in medical science, this lecture provides clear explanations, detailed diagrams, and valuable insights into female reproductive system. Enhance your knowledge and understanding of this essential aspect of human biology.
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TEST BANK For An Introduction to Brain and Behavior, 7th Edition by Bryan Kolb, Ian Q. Whishaw, Verified Chapters 1 - 16, Complete Newest Versio
TEST BANK For An Introduction to Brain and Behavior, 7th Edition by Bryan Kolb, Ian Q. Whishaw, Verified Chapters 1 - 16, Complete Newest Version
TEST BANK For An Introduction to Brain and Behavior, 7th Edition by Bryan Kolb, Ian Q. Whishaw, Verified Chapters 1 - 16, Complete Newest Version
Vestibulocochlear Nerve by Dr. Rabia Inam Gandapore.pptx
Cv edgard english_2014
1. Edgard da Veiga Lion Neto, MD; MBA
Clinical Research Clinical Research Clinical Research Clinical Research
Rua Açatunga, 149
Campo Belo, São Paulo – SP - 04612-050
Tel (011) 5533-6201 / Cel.: (011) 99342-9036
edgard.lion@uol.com.br
Professional Profile
Clinical Clinical research
· Medicine College of the University of São Paulo (FMUSP).
· Medical Residency in Surgery at the Clinics Hospital of the FMUSP.
· M. B. A. in Marketing and Communication at ESPM
· Industrial Marketing at Wharton School of the University of Pennsylvania, USA
· Legal Medicine and Expert Testimony specialist at University of São Paulo
· Clinical science proficiency by the FMGEMS - USA
· Experience in development and managing of IITs, clinical trials phase III and IV with GCP standards.
· Years of experience with Health Authorities (ANVISA, Min. of Health) focusing new product registration and
demands solving.
· Years of knowledge in support and managing of ethical marketing for mass and specialty products.
· Active participation in multitask multifunctional international work groups with Global Medical Marketing teams.
· Years of practice in the development and managing of product Advisory Boards, support to continuous medical
education, and support to patient associations.
· Experience in sales force, medical doctors and scientific medical liaisons training towards products detailing.
· Experience as a MSL and in co-managing MSLs.
· Fluent english
Languages
· English: fluent
· Spanish: basic
· French: basic
PROFISSIONAL HISTORY
Clinical Research, clinical research
Hypermarcas – Respiratory care – August 2014
Main contributions:
· Technical support to Marketing on all promotional activities with respiratory drugs for asthma and COPD according
to company compliance HA rules.
· Technical and scientific support for marketing strategies implementation.
· Revision of package inserts and scientific support for DRA and Customer Services department.
2. · Training of the sales force in all technical and clinical details of the drugs under my responsibility and their direct
competition.
· Translating medical knowledge into support and development strategy for the products within the respiratory line.
· Revision and approval of all promotional aids.
· Technical/scientific support for revision and approval of promotional aids and strategic revision of medical
literature searching for product competitive advantages in product promotion.
· Training and development of sales force towards product detailing and competitors.
· .Transformation of medical/scientific data on published articles into useful tools for promotion of respiratory
products and differentiation of the competition.
· Content development for scientific symposia and other scientific meeting.
· Package insert and other regulatory documentation revision.
· Identification of medical topics of interest for the medical community focusing the development of medical Science
programs including advisory boards.
Sanofi – MSL Oncology – May 2013
Report: Group Medical Manager
Main contributions:
· Technical detailing of clinical trials and clinical characteristics of therapeutic agents (chemotherapy and immune
biologic drugs) designed for solid tumors (Prostate and Colon).
· Scientific relationship with top KOLs, KDM and ROLs in hospitals and clinics.
· Training of technical sales consultants.
· Scientific relationship with medical societies.
· Developing of clinical trials and IST/IIT trials with KOLs.
· Scientific discussion of key messages with KOLs, KDMs and ROLs on chemotherapy and immune biologic drugs
for Prostate and Colon cancer.
· Extensive participation on international meeting and congresses.
Boehringer-Ingelheim – Neurology, Urology e Antibiotics – March 2013
Report : Chief Scientific Oficer
Main contributions:
· Technical support to Marketing on all promotional activities with drugs for Parkinson Disease, Prostate Benign
Hyperplasia and antibiotics.
· Technical support for regulatory affairs concerning new products registration and HA demands solving.
· Training of the sales force in all technical and clinical details of the drugs under my responsibility and their direct
competition.
· Coordination of technical translations.
· Technical and scientific support for marketing strategies implementation.
· Revision of package inserts and scientific support for DRA and Customer Services department.
· Technical and scientific support for all promotional activities of the products under my responsibility.
Novartis –Ophthalmology, Mature products and OCT– Jan 2004 / Jul 2012
Report : Chief Scientific Officer
Main contributions:
Strategic support to the Specialty Business Unit (Ophthalmology) and Mature Products:
· Development and implementation of clinical research projects (compassionate use, IIT and phase III /
IV) with immune biological products.
· Execution of the medical publication plan through educational support to independent studies (IITs) in
line with global strategies.
· Scientific consulting for corporate affairs and public relations with Health Authorities, Ministry of Health
and patient associations.
· Technical/scientific support for revision and approval of promotional aids and strategic revision of
medical literature searching for product competitive advantages in product promotion.
3. · Technical/scientific support to continuing medical education, workshops, satellite symposia and other
medical events.
· Revision and approval of promotional material, strategic revision of medical literature in order to localize
technical details to differentiate the company products.
· Technical support for implementation of marketing strategies with immune biologic and mature products.
· Medical Advisor for LatAm mature products (three years in the position).
· Technical support and scientific identification of new business (BD&L) looking for joint ventures in
product development and partnetships.Direct involvement in scientific consulting corporate affairs with
opinion leaders and patient associations.
· Training and development of sales force and scientific consulting force (MSLs) towards product detailing
and competitors.
· Co-managing of MSLs.
· Training of opinion leaders.
· Scientific Strategic and operational support for DRA and Market Access.
· Active participation on national and international events.
· Medical manager for Antiinflamatory/analgesic, Central Nervous System, Cardiology, Dermatology,
Ophthalmology and Mature Products
· MSL for Cardiology, Rheumatology and Orthopedy.
Aché Laboratórios – Abr 2001 / Out 2003
Clinical research, clinical research, Clinical research, Clinical Research
Report : Executive director of Marketing and sales
Main contributions:
· Supervision of five medical managers, one pharmacovigilance manager and one clinical research manager.
· Scientific support for marketing strategy implementation.
· Creation of the pharmacovigilance department.
· Strategic development of clinical research projects, identifications of investigators and research centers.
· Strategic and operational support for DRA and Market Access.
· Support for marketing and corporate public relations strategies.
· Technical support and scientific identification of new business (BD&L) looking for joint ventures in product
development and partnerships together with McKinsey Management Consulting Firm (over 1,000 new
molecules and SKUs overseen).
· Technical/scientific support for licensing in of new molecules and development of combination of molecules
as new products including synthetic and phytomedications.
· Active participation with HA discussions and negotiations.
· Active participation on national scientific events.
Searle Monsanto – Jan 1999 / Dez 2000
Clinical research, clinical research, Clinical research, Clinical Research
Report : Chief Clinical Scientific Officer LatAm/Asia-Pacific
Main contributions :
· Direct participation on scientific consulting, public relations, and training of opinion leaders.
· Technical support for the launching of the first COXIB in the market (Celecoxib).
· Training Medical leader for the COXIB products in LatAm.
· Technical support for the marketing area in promotional activities.
· Sales force training and development.
· Clinical research development, protocol writing, CRFs and diaries writing.
· Identification of investigators and clinical research centers.
· Implementation and conduction of phase IV clinical trials.
· Strategic and operational support for DRA.
· Training and development of opinion leaders.
· Active participation on national and international scientific events.
Pfizer – Abr 1997 / Dez 1998
Clinical research, clinical research, Clinical research, Clinical Research
Report : Clinical Scientific Officer
Main contributions :
4. · Scientific and operational support for marketing promotional activities.
· Development and implementation of Central Nervous System clinical research projects (phase III / IV).
· Training and development of sales force.
· Coordination of clinical research associates.
· Coordination of scientific translations.
· Protocol, CRFs and diaries development.
· Identification of investigators and clinical research centers.
Schering - Plough – Abr 1996 / Abr 1997
Clinical research, clinical research, Clinical research, Clinical Research
Report : Chief Scientific Officer
Main contributions :
· Scientific and operational support for marketing promotional activities.
· Training and development of sales force.
· Strategic and operational support for DRA.
· Protocol, CRFs and diaries development.
· Technical support and scientific identification of new business (BD&L) looking for joint ventures in product
development and partnerships.
· Development and implementation of clinical research projects (phase III / IV).
· Identification of investigators and clinical research centers.
· Active participation on national scientific events.
Sul América Aetna Insurance – Jan 1995 / Dez 1996
Report : Medical Superintendent
Main contributions :
· Teams supervision:
- Five local medical analysts for assessment of personal and company health providers.
- Twenty five medical audits at national level.
- Technical support to reimbursement and debt department.
· Technical support to the vice presidency and legal department.
· Active participation on new product development.
· Training of medical analysts.
GRADUATION
· Eletrotechnics at Federal School of São Paulo - 1981
· Medicine college of the University of São Paulo - 1988
· Medical Residency in Surgery at the Clinics Hospital - 1992
· Medical proficiency by the Educational Commission of Foreign Medical Graduates (FMGEMS), USA (1992)
· Specialization on Hospital administration (CEDAS) – São Camilo - 1994
· Specialization on Marketing administration (FEA-USP) – 1995
· 100 IMS pharmaceutic marketing - 1996
· Field Monitoring and Medical Orientation Seminar at Pfizer, Inc, New York.; Product Management Development
at Pfizer (RJ) – 1997
· Industrial Marketing at Wharton School of the University of Pennsylvania, USA.;
· Social Styles at Monsanto in Toronto, Canadá – 1999.
· Statistical methods in clinical research (SBPPC) – 2001.
· Biostatistics UNIFESP – 2002
· Certification on ICH-GCP Clinical Research by the Novartis International Clinical Research Organization - 2006
· M.B.A in Marketing and Communication - ESPM – 2006
· Legal Medicine and Expert Testimony specialization – University of Sao Paulo - 2013
5. CLINICAL EXPERIENCE
· Private office – 1990 - 1995
· HMO medical surgeon - Grupo Eluma – 1992 - 1995
· Emergency medicine - SAMEB – 1994 - 1997
SOCIETIES
· Member of the Sociedade Brasileira de Medicina Farmacêutica (SBMF)
· Coordinator of the IT committee - SBMF
· First Secretary - SBMF (2006-2007)
TITLES
· Proficiency in Medicine by the Educational Commission of Foreign Medical Graduates (FMGEMS), USA (1992)
· International Clinical Research / ICH-GCP Compliance by Novartis International Clinical Research Organization
(ICRO)
PUBLICATIONS
Avaliaçäo do DNA pela citofotometria nos tumores papiliferos da tireoide / DNA evaluation by cytophotometry in papillary
thyroid tumour
Rev. Col. Bras. Cir; 17(5):90-3, set-out. 1990.
RECOMENDATIONS
· Ricardo Maykot, MBA (Marketing and sales executive Director Novartis): Edgard has a robust background in
several therapeutic areas, a good sense of medical-marketing strategies which enable him for various
positions in the pharma industry. Extremely reliable, good player working in teams, he conquered my respect
and trust."
· Leandro Mattos Boer Martins, MD, PhD (Medical Specialist Novartis USA): "Edgar is an experienced,
proactive and tireless contributor who makes great addition to any medical team. He always completes his
assignments on time with excellence and is committed to the team in times of very difficult challenges and
corporative overturns. I would highly recommend him for any medical position in the pharmaceutical
industry."
· Felipe Pinho, MD, PhD (Diretor Médico Instituto do Sono - UNIFESP): "I worked with Edgard in Schering-
Plough. He has the two most important skills to work in a pharmaceutical company: high level technical
knowledge and impeccable ethical values."
· - Alvaro Cavalcante (Gerente de Produtos Novartis): "Edgard é um profissional multifuncional, com sólida
experiência em diversas áreas terapêuticas. Tem perfil "hands on" e rapidamente se adapta a estrutura de
negócio."
· Leonardo Mallmann (Senior Marketing Manager for HIV - Virology at Merck): "Dr. Edgard is a detail-oriented
medical manager who doesn´t lose sight of the strategic objective and is focused on growing the business.
· Julio Madi (Sr. Medical Adviser at Hypermarcas S/A): “Edgard is a well-known medical manager at the
pharma industry. He is an "easy to work with" person who can challenge you in a positive and result-oriented
way. Always looking ahead, he is nice as a medical-marketing team player in different therapeutic areas.”
6. · David Lago (Legal Director Safra Bank, former Senior Legal Manager Novartis): "Edgard is an outstanding
professional, highly competent and committed, with wide experience as Medical Manager. He has very good
relationship with his colleagues and focus on the company’s targets."
· Renata Berardocco, PharmD (Project Director & Head of Brazil at Covance): "Edgard is a very good
professional and results oriented. He is a pleasant person to work with and a good team player."
REFERENCES
· Silvia Sfeir (Director of Market Access, Public Commercial Sales, Health Economics, BD&L and New
Products Planning Novartis): Silvia.sfeir@novartis.com Phone +55 11 55327122 Cell: 99656-1036.
· Patricia Pigola, PharmD (Director of Regulatory Affairs da Novartis): patricia.pigola@novartis.com Phone +
55 11 55327590
· João Navarro, MD, MBA (Sanofi LatAm Medical Manager), joao.navarro@sanofi.com.br, phone: 55 11
37596726
· Felipe Dos Santos Pinho, MD, PhD (Instituto do Sono - UNIFESP ): f.spinho@uol.com.br ou
felipe.pinho@ems.com.br Phone 55 19 92127964
· Ricardo Maykot (Executive Director, Commercial Operations, Innovation and BU support, Novartis):
ricardo.maykot@novartis.com Phone +55 11 5532-7713
· Leandro Martins, MD, PhD (Medical Specialist Novartis New Jersey, NJ, USA):
leandro.martins@novartis.com Phone +1 862 7783959
7. · David Lago (Legal Director Safra Bank, former Senior Legal Manager Novartis): "Edgard is an outstanding
professional, highly competent and committed, with wide experience as Medical Manager. He has very good
relationship with his colleagues and focus on the company’s targets."
· Renata Berardocco, PharmD (Project Director & Head of Brazil at Covance): "Edgard is a very good
professional and results oriented. He is a pleasant person to work with and a good team player."
REFERENCES
· Silvia Sfeir (Director of Market Access, Public Commercial Sales, Health Economics, BD&L and New
Products Planning Novartis): Silvia.sfeir@novartis.com Phone +55 11 55327122 Cell: 99656-1036.
· Patricia Pigola, PharmD (Director of Regulatory Affairs da Novartis): patricia.pigola@novartis.com Phone +
55 11 55327590
· João Navarro, MD, MBA (Sanofi LatAm Medical Manager), joao.navarro@sanofi.com.br, phone: 55 11
37596726
· Felipe Dos Santos Pinho, MD, PhD (Instituto do Sono - UNIFESP ): f.spinho@uol.com.br ou
felipe.pinho@ems.com.br Phone 55 19 92127964
· Ricardo Maykot (Executive Director, Commercial Operations, Innovation and BU support, Novartis):
ricardo.maykot@novartis.com Phone +55 11 5532-7713
· Leandro Martins, MD, PhD (Medical Specialist Novartis New Jersey, NJ, USA):
leandro.martins@novartis.com Phone +1 862 7783959