#TuracozHealthcareSolutions provides support in conducting #MedicalAdvisoryBoardMeetings, and talks about the importance of #MedicalWriting for such meetings.
Benchmarking Advisory Board Management At Large Pharmaceutical And Medical De...Best Practices
Pharmaceutical advisory boards provide strategic inputs and guidance to organizations on various business aspects. However, successful advisory board management requires optimum investment in resources and operations. To maximize the return on investment it is important for pharmaceutical and medical device professionals to ensure that the quality of meetings and dialogue with advisory boards is excellent.
This research from Best Practices, LLC is designed for pharmaceutical and biotech executives seeking ways to best utilize the knowledge of advisory boards. Research findings provide benchmarks on the appropriate structure for various types of advisory boards, selection of advisory board participants, advisory board operational and resource benchmarks.
Method, tools and recommendations to boost Medical Science Liaisons Competence and performance.
Presentation of best practices to manage key opinion leaders
"What is a Medical Science Liaison ?" * "Medical Science Liaison"
Have you always wanted to know...What is a Medical Science Liaison? What do Medical Science Liaisons actually do? What is their Roles & Responsibility? What are the various alternative job titles for the MSL? How do I break into the MSL role? Find out...
If you like this presentation-PLEASE like it!
Introduction to ICSR Narrative Writing in Drug Safety & Pharmacovigilance in Pharmaceuticals, Bio-Pharmaceuticals, Medical Devices, Cosmeceuticals and Foods.
Contact:
"Katalyst Healthcares & Life Sciences"
South Plainfield, NJ, USA
info@KatalystHLS.com
Benchmarking Advisory Board Management At Large Pharmaceutical And Medical De...Best Practices
Pharmaceutical advisory boards provide strategic inputs and guidance to organizations on various business aspects. However, successful advisory board management requires optimum investment in resources and operations. To maximize the return on investment it is important for pharmaceutical and medical device professionals to ensure that the quality of meetings and dialogue with advisory boards is excellent.
This research from Best Practices, LLC is designed for pharmaceutical and biotech executives seeking ways to best utilize the knowledge of advisory boards. Research findings provide benchmarks on the appropriate structure for various types of advisory boards, selection of advisory board participants, advisory board operational and resource benchmarks.
Method, tools and recommendations to boost Medical Science Liaisons Competence and performance.
Presentation of best practices to manage key opinion leaders
"What is a Medical Science Liaison ?" * "Medical Science Liaison"
Have you always wanted to know...What is a Medical Science Liaison? What do Medical Science Liaisons actually do? What is their Roles & Responsibility? What are the various alternative job titles for the MSL? How do I break into the MSL role? Find out...
If you like this presentation-PLEASE like it!
Introduction to ICSR Narrative Writing in Drug Safety & Pharmacovigilance in Pharmaceuticals, Bio-Pharmaceuticals, Medical Devices, Cosmeceuticals and Foods.
Contact:
"Katalyst Healthcares & Life Sciences"
South Plainfield, NJ, USA
info@KatalystHLS.com
Pre-Launch Planning: Priming Your Pharma Brand For Profit And Success (mini)Eularis
In today’s environment, Pharmaceutical companies find themselves in a bind. Until recently, if drugs made over $500 Million in annual revenue within 3 to 5 years of launch, they were considered hugely successful. They were a support to an extensive company portfolio and a component of greater company profit.
However, things have changed. The standards for a successful drug have become much higher and much more dangerous. With so many revenue-producing drugs going off patent, companies are facing large holes in their balance sheets and sales that are increasingly slow.
Plus, with the stakes high and available funds low, pipelines are drying up. Add to this the closer scrutiny of safety issues, the rise of Generics, slower physician acceptance and adoption of new therapies, and the Pharma Industry is in trouble.
More and more, companies are expecting marketers to be instrumental at the key moment of launch, and marketers are under extreme pressure. To deliver on the high hopes of Pharmaceutical brand launch, companies must engage in comprehensive pre-launch planning.
In this report we analyze why launch is increasingly important, the issues involved in pre-launch planning, including key organizational strategies, marketing tactics, regulatory considerations, global issues, and methods for ensuring the most effective plans.
Visdios is a specialist in key opinion leader management, development, implement process and also manage all kind of KOL solutions across your company. We engage with our valuable customers to get a real understanding of their business requirements.
http://visdios.com/kol-management-india/
Medical manuscript writing is a document that depicts the research done by the researcher. It should be accurate, complete, precise, and provide unambiguous information.
https://www.cognibrain.com/medical-manuscript-all-you-need-to-know-about/
“CSR is a detailed regulatory document which gives the information about the methods and results (related to efficacy and safety) of a clinical trial. CSRs are created as a part of the process of submitting applications to the Regulatory Authorities for new medical treatments and for its approval. CSRs can be full, abbreviated, synopsis, supplementary, observational etc as per the results and requirements”.
The basics of launching a pharmaceutical drug-
Based on studies done on the practices of 13 top pharmaceutical companies in the world.
For more, write to info@markivmedical.com
Regulatory medical writing is an integral part of Medical Communications, but is often overlooked. In simple terms, it involves writing of the documents required for the approval of drugs by the regulatory authorities.
https://www.cognibrain.com/regulatory-medical-writing/
Functions in Medical Affairs, Medical Information Enquiries , PowerPoint Requests , Meeting with doctors , In-clinic effectiveness , Questionnaire and Surveys, Training , New Brand Launch, Hierarchy , Work Management
Training Program for Medical Representatives by Anup Soans Anup Soans
“Hardknocks for GreenHorn is a good book and very useful tool for any one starting his / her career in Pharma Industry..
It covers all basic concepts i.e Medical Part, Sales Tools, Innovative methods and much more. I strongly recommend this book to be the part of freshers training batch in any Pharma Company. .”
Pharmacovigilance Process Work Flow - Katalyst HLSKatalyst HLS
Introduction to Drug Safety & Pharmacovigilance Process Work Flow for Pharmaceuticals, Bio-Pharmaceuticals, Medical Devices, Cosmeceuticals and Foods.
Contact:
"Katalyst Healthcares & Life Sciences"
South Plainfield, NJ, USA
info@KatalystHLS.com
SAE REPORTING TIMELINE AND COMPENSATION 2019Shweta Lal
This presentation is based on New Drug and Clinical Trial Rule 2019 which was published in 19 march 2019. I have described chapter VI ( compensation) and Seventh Schedule including SAE reporting timeline in India.
Understanding Contracts in the Clinical Research ProcessMichael Swit
Presentation on key aspects of clinical trial agreements, with an emphasis on clauses impacting indemnification, confidentiality, material transfers, record retention, ownership of data,
Medical writing is the art of creating a document that includes medical information in a readable language which is easily comprehended by the target audience. The target audience for medical writing varies and so is the style of medical writing.
https://www.cognibrain.com/medical-writing-answering-your-questions/
Better Healthcare Through Community and Stakeholder Engagement, 2015 Webinar ...Paul Gallant
"An enjoyable presentation, well-delivered with excellent insight into community and stakeholder engagement strategies. Terry Dyni - July 23, 2015" on the webinar version. This version is my complete slide deck from a live webinar presentation requested by the Conference Board of Canada. April, 2015. Thanks for your interest in Better Healthcare Through Community and Stakeholder Engagement.
Compliments of Paul W. Gallant, CHE, GALLANT HEALTHWORKS & Associates (GHWA), Vancouver, BC, Canada. PS See the last slide for contact details or to arrange customized training/facilitation or advice on your organizational needs.
Pre-Launch Planning: Priming Your Pharma Brand For Profit And Success (mini)Eularis
In today’s environment, Pharmaceutical companies find themselves in a bind. Until recently, if drugs made over $500 Million in annual revenue within 3 to 5 years of launch, they were considered hugely successful. They were a support to an extensive company portfolio and a component of greater company profit.
However, things have changed. The standards for a successful drug have become much higher and much more dangerous. With so many revenue-producing drugs going off patent, companies are facing large holes in their balance sheets and sales that are increasingly slow.
Plus, with the stakes high and available funds low, pipelines are drying up. Add to this the closer scrutiny of safety issues, the rise of Generics, slower physician acceptance and adoption of new therapies, and the Pharma Industry is in trouble.
More and more, companies are expecting marketers to be instrumental at the key moment of launch, and marketers are under extreme pressure. To deliver on the high hopes of Pharmaceutical brand launch, companies must engage in comprehensive pre-launch planning.
In this report we analyze why launch is increasingly important, the issues involved in pre-launch planning, including key organizational strategies, marketing tactics, regulatory considerations, global issues, and methods for ensuring the most effective plans.
Visdios is a specialist in key opinion leader management, development, implement process and also manage all kind of KOL solutions across your company. We engage with our valuable customers to get a real understanding of their business requirements.
http://visdios.com/kol-management-india/
Medical manuscript writing is a document that depicts the research done by the researcher. It should be accurate, complete, precise, and provide unambiguous information.
https://www.cognibrain.com/medical-manuscript-all-you-need-to-know-about/
“CSR is a detailed regulatory document which gives the information about the methods and results (related to efficacy and safety) of a clinical trial. CSRs are created as a part of the process of submitting applications to the Regulatory Authorities for new medical treatments and for its approval. CSRs can be full, abbreviated, synopsis, supplementary, observational etc as per the results and requirements”.
The basics of launching a pharmaceutical drug-
Based on studies done on the practices of 13 top pharmaceutical companies in the world.
For more, write to info@markivmedical.com
Regulatory medical writing is an integral part of Medical Communications, but is often overlooked. In simple terms, it involves writing of the documents required for the approval of drugs by the regulatory authorities.
https://www.cognibrain.com/regulatory-medical-writing/
Functions in Medical Affairs, Medical Information Enquiries , PowerPoint Requests , Meeting with doctors , In-clinic effectiveness , Questionnaire and Surveys, Training , New Brand Launch, Hierarchy , Work Management
Training Program for Medical Representatives by Anup Soans Anup Soans
“Hardknocks for GreenHorn is a good book and very useful tool for any one starting his / her career in Pharma Industry..
It covers all basic concepts i.e Medical Part, Sales Tools, Innovative methods and much more. I strongly recommend this book to be the part of freshers training batch in any Pharma Company. .”
Pharmacovigilance Process Work Flow - Katalyst HLSKatalyst HLS
Introduction to Drug Safety & Pharmacovigilance Process Work Flow for Pharmaceuticals, Bio-Pharmaceuticals, Medical Devices, Cosmeceuticals and Foods.
Contact:
"Katalyst Healthcares & Life Sciences"
South Plainfield, NJ, USA
info@KatalystHLS.com
SAE REPORTING TIMELINE AND COMPENSATION 2019Shweta Lal
This presentation is based on New Drug and Clinical Trial Rule 2019 which was published in 19 march 2019. I have described chapter VI ( compensation) and Seventh Schedule including SAE reporting timeline in India.
Understanding Contracts in the Clinical Research ProcessMichael Swit
Presentation on key aspects of clinical trial agreements, with an emphasis on clauses impacting indemnification, confidentiality, material transfers, record retention, ownership of data,
Medical writing is the art of creating a document that includes medical information in a readable language which is easily comprehended by the target audience. The target audience for medical writing varies and so is the style of medical writing.
https://www.cognibrain.com/medical-writing-answering-your-questions/
Better Healthcare Through Community and Stakeholder Engagement, 2015 Webinar ...Paul Gallant
"An enjoyable presentation, well-delivered with excellent insight into community and stakeholder engagement strategies. Terry Dyni - July 23, 2015" on the webinar version. This version is my complete slide deck from a live webinar presentation requested by the Conference Board of Canada. April, 2015. Thanks for your interest in Better Healthcare Through Community and Stakeholder Engagement.
Compliments of Paul W. Gallant, CHE, GALLANT HEALTHWORKS & Associates (GHWA), Vancouver, BC, Canada. PS See the last slide for contact details or to arrange customized training/facilitation or advice on your organizational needs.
Presented at the 2014 Los Angeles County Psychological Association's Convention. Basics of ethical paperwork in private practice for mental health professionals.
Start the Discussion: The Importance of Advance DirectivesSummit Health
We will discuss the importance of planning ahead about end-of-life decisions, provide useful information about how to prepare advance directives, and distribute sample forms.
Planning and Conducting Advocacy at National and Subnational LevelsCORE Group
Fall Global Health Practitioner Conference 2017
Planning and Conducting Advocacy at National and Subnational Levels
Kavita Sethuraman, Annie Toro, & Danielle Heilberg
Taking minutes at meetings is one way for health centers to demonstrate compliance in a variety of areas. However, sometimes minute taking isn’t easy; minutes can often lack documentation, or may not express what actually transpired with a discussion. This session will provide participants with the following:
Understanding why meeting minutes are important for HRSA compliance
Identifying what should be included in meeting minutes for topics such as Quality, Sliding Fee Discount Program and Governance
Examples of meeting minutes that can be utilized to develop best practices
Compliatric webinar series strategies for effective meeting minutesCompliatric
Taking minutes at meetings is one way for health centers to demonstrate compliance in a variety of areas. However, sometimes minute taking isn’t easy; minutes can often lack documentation, or may not express what actually transpired with a discussion. This session will provide participants with the following:
Understanding why meeting minutes are important for HRSA compliance
Identifying what should be included in meeting minutes for topics such as Quality, Sliding Fee Discount Program and Governance
Examples of meeting minutes that can be utilized to develop best practices
How to get the most of EHA as a patient advocatejangeissler
"How to get the most of EHA as a patient advocate", presented by Jan Geissler at the EHA / EuroBloodNet Capacity Building Meeting for Patient Advocates on 22 June 2017, Madrid
This slide deck is about Prostate cancer. It is amongst the leading cause of cancer deaths in adult males. This slide deck will provide you with necessary information regarding the symptoms, risk, diagnosis, and possible treatment of prostate cancer. I hope the readers find this slide deck useful & informative
To clear your queries like,
What is prescription drug overdose?
Why you need to know?
Drug overdose deaths worldwide
Reasons for prescription drug overdose
Accidental drug overdose
Accidental drug overdose – what can you do?
Intentional drug overdose
Many employees are now based at home or work remotely in turns, while employees with serious health conditions and pregnant or breastfeeding women may continue to work at home, for the foreseeable future...Read more from slides
Turacoz Healthcare Solutions provides clinical research and regulatory writing services for pharmaceutical companies. We tell you about the different components of a clinical study protocol, the document which is prepared before beginning of any clinical trial. To know more info, visit- goo.gl/C1ec0L or write to us at hello@turacoz.in and call us 011-40584280.
Before the enrollment of a patient in a clinical trial and beginning of any trial-related procedures, an informed consent is obtained from the potential participants. This informed consent form (ICF) provides the participants with the information related to the clinical trial. TSDP provides regulatory medical writing training on preparation of ICF.
Editing helps to make a manuscript consistent, correct and clear, thus improving its readability and communication. In this slideshare, Turacoz shares certain tips that will definitely enrich the knowledge of medical writers to help gain a good understanding of editing.
“Regulatory writing department at Turacoz have the expertise to develop various regulatory documents such as Investigator Brochures (IBs), Protocols, Clinical Study Reports (CSRs), Common Technical Documents (CTDs) and pharmacovigilance documents such as Periodic Safety Update Reports (PSURs) and Risk Management Plans (RMPs). In these slides, we have presented an overview on Periodic safety update reports (PSURs) and also the guidelines such GVP modules and ICH E2c. We have also discussed the changes from old PSUR format to new Periodic Benefit-Risk Evaluation Report (PBRER) format.”
Turacoz Healthcare Solutions - Risk management plan is one of the many documents that come under regulatory writing. It is meant to be submitted to the health authorities during the process of gaining market authorization or at the time of any safety updates to the medicinal product.
Trauma Outpatient Center is a comprehensive facility dedicated to addressing mental health challenges and providing medication-assisted treatment. We offer a diverse range of services aimed at assisting individuals in overcoming addiction, mental health disorders, and related obstacles. Our team consists of seasoned professionals who are both experienced and compassionate, committed to delivering the highest standard of care to our clients. By utilizing evidence-based treatment methods, we strive to help our clients achieve their goals and lead healthier, more fulfilling lives.
Our mission is to provide a safe and supportive environment where our clients can receive the highest quality of care. We are dedicated to assisting our clients in reaching their objectives and improving their overall well-being. We prioritize our clients' needs and individualize treatment plans to ensure they receive tailored care. Our approach is rooted in evidence-based practices proven effective in treating addiction and mental health disorders.
INFECTION OF THE BRAIN -ENCEPHALITIS ( PPT)blessyjannu21
Neurological system includes brain and spinal cord. It plays an important role in functioning of our body. Encephalitis is the inflammation of the brain. Causes include viral infections, infections from insect bites or an autoimmune reaction that affects the brain. It can be life-threatening or cause long-term complications. Treatment varies, but most people require hospitalization so they can receive intensive treatment, including life support.
Rate Controlled Drug Delivery Systems, Activation Modulated Drug Delivery Systems, Mechanically activated, pH activated, Enzyme activated, Osmotic activated Drug Delivery Systems, Feedback regulated Drug Delivery Systems systems are discussed here.
Feeding plate for a newborn with Cleft Palate.pptxSatvikaPrasad
A feeding plate is a prosthetic device used for newborns with a cleft palate to assist in feeding and improve nutrition intake. From a prosthodontic perspective, this plate acts as a barrier between the oral and nasal cavities, facilitating effective sucking and swallowing by providing a more normal anatomical structure. It helps to prevent milk from entering the nasal passage, thereby reducing the risk of aspiration and enhancing the infant's ability to feed efficiently. The feeding plate also aids in the development of the oral muscles and can contribute to better growth and weight gain. Its custom fabrication and proper fitting by a prosthodontist are crucial for ensuring comfort and functionality, as well as for minimizing potential complications. Early intervention with a feeding plate can significantly improve the quality of life for both the infant and the parents.
Dr. David Greene R3 stem cell Breakthroughs: Stem Cell Therapy in CardiologyR3 Stem Cell
Dr. David Greene, founder and CEO of R3 Stem Cell, is at the forefront of groundbreaking research in the field of cardiology, focusing on the transformative potential of stem cell therapy. His latest work emphasizes innovative approaches to treating heart disease, aiming to repair damaged heart tissue and improve heart function through the use of advanced stem cell techniques. This research promises not only to enhance the quality of life for patients with chronic heart conditions but also to pave the way for new, more effective treatments. Dr. Greene's work is notable for its focus on safety, efficacy, and the potential to significantly reduce the need for invasive surgeries and long-term medication, positioning stem cell therapy as a key player in the future of cardiac care.
This document is designed as an introductory to medical students,nursing students,midwives or other healthcare trainees to improve their understanding about how health system in Sri Lanka cares children health.
Deep Leg Vein Thrombosis (DVT): Meaning, Causes, Symptoms, Treatment, and Mor...The Lifesciences Magazine
Deep Leg Vein Thrombosis occurs when a blood clot forms in one or more of the deep veins in the legs. These clots can impede blood flow, leading to severe complications.
Letter to MREC - application to conduct studyAzreen Aj
Application to conduct study on research title 'Awareness and knowledge of oral cancer and precancer among dental outpatient in Klinik Pergigian Merlimau, Melaka'
The dimensions of healthcare quality refer to various attributes or aspects that define the standard of healthcare services. These dimensions are used to evaluate, measure, and improve the quality of care provided to patients. A comprehensive understanding of these dimensions ensures that healthcare systems can address various aspects of patient care effectively and holistically. Dimensions of Healthcare Quality and Performance of care include the following; Appropriateness, Availability, Competence, Continuity, Effectiveness, Efficiency, Efficacy, Prevention, Respect and Care, Safety as well as Timeliness.
2. Introduction to Advisory Board
• An ‘Advisory board’ is a body of key opinion leaders (KOLs) in the company’s fields of
expertise which is formed in order to obtain valuable insights on various aspects
related to a product or disease state
• KOLs are either selected by the pharmaceutical companies or by medical societies
related to the therapeutic area
3. Composition of a Medical Advisory Board
Chairperson
KOLs Medical Advisors
Medical affair
professionals of
pharma company
4. Purpose of Conducting Advisory Board Meetings
For knowledge sharing with healthcare stakeholders of a pharma
For gaining non-binding but informed guidance on various business
aspects of a drug/product/services
For better understanding and interpretation of the various medical
benefits/limitations of a drug/product/service
For getting prior insights on possible research opportunities, including
guidance on the clinical development and trial protocols, as well as
health care needs that might drive future clinical strategies
5. Organizers of Advisory Board Meetings
Pharmaceutical Companies
Sponsored/Non-sponsored Medical Societies
Medical Communication Companies
Publication Houses
6. Role of a Medical Writer in Advisory Board Meeting
Engaging KOLs for
an advisory board
Preparing
questionnaires
Conducting online
surveys (for
understanding
unmet needs)
Preparing a pre-
meeting report to
be shared with
KOLs
Preparing
presentations for
the advisory board
meeting
Hosting an
advisory board
Capturing minutes
of meeting
Preparing draft for
meeting report
Modifying the
report into a
publication-ready
literature
7. Documents Prepared by a Medical Writer During Advisory
Board Meeting
Pre-Meeting
• Questionnaires
• Presentations
• Posters
• Pre-meeting report
During Meeting
• Notes of the discussion
Post-Meeting
• Minutes of Meeting
• Final Report
• Good clinical practice
• Clinical recommendations
• Consensus statements
• Treatment guidelines/
policies
• Expert opinion
• Executive summary
8. Preparing for Attending an Advisory Board Meeting
• Have a clear communication with client/organizing body about the objective of the
meeting
• Do a literature search to get acquainted with the therapeutic area of the advisory board
• If meeting is an extension of the previous meetings, ask client to share the report of
previous meetings
• Ask the client if any other assistance is needed by the medical writer before the
advisory board meeting e.g. preparing presentations, delivering presentations,
preparing a questionnaire for the survey etc.
• Ask about the availability of video/audio recording at the meeting
• Get acquainted with the participating members of the advisory board, if permissible,
discuss with them the objectives and their expectations from the advisory board
9. Attending Advisory Board and Writing Minutes of Meeting
• Be attentive during the meeting and capture all the important points discussed
• Audio and video recordings of the meeting are helpful, but always take down your own
notes at meeting
• In case you missed out any specific point, contact the concerned person soon after the
meeting to collect the missing information
• It is advisable to write minutes of meeting soon after you attended the meeting
• Minutes of meeting should include particulars about the meeting, information about the
organizing body and the participating KOLs, background information about the unmet need
that is to be discussed, objective of the meeting, highlights of the discussion, and future
directions (as suggested by the KOLs)
10. Writing the Final Report
Final report should include:
• Detailed background information on the therapeutic area
• Introduction to the problem
• Current unmet needs/knowledge-practice gap among the health care practitioners
• Objective of the meeting
• Discuss the insights provided by the KOLs and support or compare them with the
available medical evidence
• Future directions or recommendations
11. Things to Remember!
• Prepare well for before attending the meeting
• Understand the need or purpose of the advisory board meeting
• Identify your scope of work
• Be informed about the important points that are to be discussed
• Be attentive during the meeting and take down proper notes
• Prepare minutes of meeting as soon as possible
• Create/prepare an objective-driven report
12. THANK YOU
Turacoz Skill Development Program
973, H-block First Floor Sector-7,
Dwarka, New Delhi-110075.
+91 – 9810036125
011 – 47039856
hello@turacoz.in
www.tmedicalwritingtraining.com