IQPC’s Cold Chain MENA summit will combine Supply Chain, Logistics and Quality leaders from Multi-national biopharma companies from the region and around the world as well as government and regulatory figures to discuss issues and proposed solutions that may occur across the supply chain.
For more information, visit www.coldchainmena.com
IQPC’s Cold Chain MENA summit will combine Supply Chain, Logistics and Quality leaders from Multi-national biopharma companies from the region and around the world as well as government and regulatory figures to discuss issues and proposed solutions that may occur across the supply chain.
For more information, visit www.coldchainmena.com
Ocasa Logistics Solutions
Bio-Genetic logistics, import and export of medical supplies, medication, extraction kits and related materials for clinical trials worldwide under various conditions: at room temperature, refrigerated, or frozen, with ordinary or dry ice, depending on the specifications for each sample to pharmaceutical companies, CRO’s, or medical centers abroad.
P-VALUE MEDICAL is an independent Contract
Research Organization whose main aim is to
encourage and provide exceptional research
services to our clients. Our commitment is to help
Pharmaceutical research, diagnostic and
biotechnology companies to develop clinical trials
and other pertinent studies in order to introduce
their products or their new indications in the
market.
ClinActis Pte Ltd is a full service CRO providing clinical trial services to the pharmaceutical, medical device, medical nutrition and biotech companies in Asia Pacific. Established in 2009, ClinActis Pte Ltd is headquartered in Singapore.
ClinActis Experience
• 45 years experience in clinical research in pharmaceutical and biotechnology companies as well as CROs
• 27 years experience in Asia Pacific, including Australia/New Zealand, China, Malaysia, Hong Kong, India, Indonesia, The Philippines, Singapore, South Korea, Taiwan, Thailand and Japan
• Extensive knowledge of regulatory frameworks, best KOLs and sites across the region
• Vast therapeutic experience including Cardiovascular, CNS, Endocrinology, Infectious diseases, Oncology, and Respiratory
KPS Clinical Services (KPSCS) is set up by the RAHE Group of Organizations, with an aim to become one of the India's leading research-based Contract Research Organization (CRO). Our commitment is to improve the quality of human life & to provide world class clinical research services to pharmaceutical, biotechnology, medical device companies, academic and government organizations.
We wish to focus on the prevailing issues in clinical research & give their solutions with a fresh and rational approach. In this endeavor, we have successfully established a team of highly qualified and experienced multi-disciplinary GCP trained personnel. The services provided by KPSCS are knowledge-driven and based on the understanding of the pharmacology and molecular basis of disease. We believe in providing quality services & we prioritize customer relationships.
AHMC’s successful track record includes collaboration in more than 50 hospitals and projects spanning 24 countries around the world. AHMC’s hospital network consists of 32 hospital and healthcare centers, among them 13 operational facilities consisting of nearly 3,000 beds, 2,200 physicians and 5,500 employees which it has either invested in or currently manages.
IFPMA-TFDA Workshop on Couterfeit Medicines
‘Integrated Approach Against Fake Medicines’
Session 1: Current Regulatorz Landscape & Initiatives Against Fake Medicines
On 6th February 2015
At Taipei International Convention Center
Taipei, Taiwan
Accreditation of Inspection Activities of health and social care providers - ...Mara International
The 3rd GCC Laboratory Proficiency Conference is organized as part of the strategic orientations of the GCC Standardization
Organization (GSO) for the development of the standardization and quality infrastructure, thereby contributing to the development of commerce and industry and to the support of national economy in the GCC member states.
Since the field of proficiency testing is newly introduced in the GCC member states and as the infrastructure of laboratories has not yet taken the shape of national or regional organizations representing the laboratories and reflecting their requirements, GSO is in need of meeting with a considerable group of laboratories to explore and prioritize GCC member states’ requirements in terms of the fields which must top the list of the fields to be developed and upgraded.
Based on the study conducted by GSO during 2011 on the status of proficiency testing activities in the member states which shown that the laboratories operating in the member states are in need of a unified data center on proficiency testing activities, GSO
organized two conferences in 2013 and 2014 on the subject. The conferences scored high rates of success in terms of the selected scientific material, quality of speakers and the targeted audience.
Accordingly, GSO conceptualization of the method of coordinating and upgrading the activity of proficiency tests in the GCC member states included a recommendation on the organization of annual training courses and awareness symposia by the GSO on the fields of proficiency tests.
This year’s Conference will be held in Dubai during two days the 24th and 25th of March 2015, and will coincide with the annual Analytical Industry exhibition ARABLAB which will be held in Dubai during the period 23 – 26 March 2015.
Clinical Research Organization Services | Contract Research Company - PepgraPEPGRA Healthcare
Pepgra is a global contract research organization and drug development services company. It provides various phases of clinical research trials services to pharmaceutical and biotechnology companies to help reduce the time and costs associated with drug development.
Contact Us:
Website : https://bit.ly/33Fwsye
Email us: sales.cro@pepgra.com
India: +91 9884350006
United Kingdom: +44- 74248 10299
We are a Life Science staffing firm focused in the areas of Scientific, Clinical Research & Engineering for the US Biotech, Pharmaceutical, Medical Device and Diagnostic markets.
Service Overview
Site management services to CRO and SITE:
A) Pre initiation
Identification of Potential Sites
Faster Feasibility
Site set up, supplies and other infrastructure needs
Regulatory and IEC/ IRB communications
Rapid negotiation of CTA
Setting up Standard Operating Procedures (SOPs)
B) During Study Duration
Provide dedicated trained and experienced CRCs (Clinical research coordinators)
Patient recruitment & retention Support
Maintenance of essential documents
Source documentation as per ALCOA standards (Attributable, Legible, Contemporaneous, Original & Accurate
Regular IP (Investigational Product) accountability and storage
Completion of CRF’s within timelines
Faster query resolution
Reporting of AE, SAEs within timelines
Support Monitoring visits and Quality Assurance audit action items.
Patient visit Follow Up and compliance assistance
Preparation of site for monitoring and audits/ inspections
C) Post Close out
· Archiving of site results and documents
Site Identification
Faster Feasibility
Ready Sites
Ocasa Logistics Solutions
Bio-Genetic logistics, import and export of medical supplies, medication, extraction kits and related materials for clinical trials worldwide under various conditions: at room temperature, refrigerated, or frozen, with ordinary or dry ice, depending on the specifications for each sample to pharmaceutical companies, CRO’s, or medical centers abroad.
P-VALUE MEDICAL is an independent Contract
Research Organization whose main aim is to
encourage and provide exceptional research
services to our clients. Our commitment is to help
Pharmaceutical research, diagnostic and
biotechnology companies to develop clinical trials
and other pertinent studies in order to introduce
their products or their new indications in the
market.
ClinActis Pte Ltd is a full service CRO providing clinical trial services to the pharmaceutical, medical device, medical nutrition and biotech companies in Asia Pacific. Established in 2009, ClinActis Pte Ltd is headquartered in Singapore.
ClinActis Experience
• 45 years experience in clinical research in pharmaceutical and biotechnology companies as well as CROs
• 27 years experience in Asia Pacific, including Australia/New Zealand, China, Malaysia, Hong Kong, India, Indonesia, The Philippines, Singapore, South Korea, Taiwan, Thailand and Japan
• Extensive knowledge of regulatory frameworks, best KOLs and sites across the region
• Vast therapeutic experience including Cardiovascular, CNS, Endocrinology, Infectious diseases, Oncology, and Respiratory
KPS Clinical Services (KPSCS) is set up by the RAHE Group of Organizations, with an aim to become one of the India's leading research-based Contract Research Organization (CRO). Our commitment is to improve the quality of human life & to provide world class clinical research services to pharmaceutical, biotechnology, medical device companies, academic and government organizations.
We wish to focus on the prevailing issues in clinical research & give their solutions with a fresh and rational approach. In this endeavor, we have successfully established a team of highly qualified and experienced multi-disciplinary GCP trained personnel. The services provided by KPSCS are knowledge-driven and based on the understanding of the pharmacology and molecular basis of disease. We believe in providing quality services & we prioritize customer relationships.
AHMC’s successful track record includes collaboration in more than 50 hospitals and projects spanning 24 countries around the world. AHMC’s hospital network consists of 32 hospital and healthcare centers, among them 13 operational facilities consisting of nearly 3,000 beds, 2,200 physicians and 5,500 employees which it has either invested in or currently manages.
IFPMA-TFDA Workshop on Couterfeit Medicines
‘Integrated Approach Against Fake Medicines’
Session 1: Current Regulatorz Landscape & Initiatives Against Fake Medicines
On 6th February 2015
At Taipei International Convention Center
Taipei, Taiwan
Accreditation of Inspection Activities of health and social care providers - ...Mara International
The 3rd GCC Laboratory Proficiency Conference is organized as part of the strategic orientations of the GCC Standardization
Organization (GSO) for the development of the standardization and quality infrastructure, thereby contributing to the development of commerce and industry and to the support of national economy in the GCC member states.
Since the field of proficiency testing is newly introduced in the GCC member states and as the infrastructure of laboratories has not yet taken the shape of national or regional organizations representing the laboratories and reflecting their requirements, GSO is in need of meeting with a considerable group of laboratories to explore and prioritize GCC member states’ requirements in terms of the fields which must top the list of the fields to be developed and upgraded.
Based on the study conducted by GSO during 2011 on the status of proficiency testing activities in the member states which shown that the laboratories operating in the member states are in need of a unified data center on proficiency testing activities, GSO
organized two conferences in 2013 and 2014 on the subject. The conferences scored high rates of success in terms of the selected scientific material, quality of speakers and the targeted audience.
Accordingly, GSO conceptualization of the method of coordinating and upgrading the activity of proficiency tests in the GCC member states included a recommendation on the organization of annual training courses and awareness symposia by the GSO on the fields of proficiency tests.
This year’s Conference will be held in Dubai during two days the 24th and 25th of March 2015, and will coincide with the annual Analytical Industry exhibition ARABLAB which will be held in Dubai during the period 23 – 26 March 2015.
Clinical Research Organization Services | Contract Research Company - PepgraPEPGRA Healthcare
Pepgra is a global contract research organization and drug development services company. It provides various phases of clinical research trials services to pharmaceutical and biotechnology companies to help reduce the time and costs associated with drug development.
Contact Us:
Website : https://bit.ly/33Fwsye
Email us: sales.cro@pepgra.com
India: +91 9884350006
United Kingdom: +44- 74248 10299
We are a Life Science staffing firm focused in the areas of Scientific, Clinical Research & Engineering for the US Biotech, Pharmaceutical, Medical Device and Diagnostic markets.
Service Overview
Site management services to CRO and SITE:
A) Pre initiation
Identification of Potential Sites
Faster Feasibility
Site set up, supplies and other infrastructure needs
Regulatory and IEC/ IRB communications
Rapid negotiation of CTA
Setting up Standard Operating Procedures (SOPs)
B) During Study Duration
Provide dedicated trained and experienced CRCs (Clinical research coordinators)
Patient recruitment & retention Support
Maintenance of essential documents
Source documentation as per ALCOA standards (Attributable, Legible, Contemporaneous, Original & Accurate
Regular IP (Investigational Product) accountability and storage
Completion of CRF’s within timelines
Faster query resolution
Reporting of AE, SAEs within timelines
Support Monitoring visits and Quality Assurance audit action items.
Patient visit Follow Up and compliance assistance
Preparation of site for monitoring and audits/ inspections
C) Post Close out
· Archiving of site results and documents
Site Identification
Faster Feasibility
Ready Sites
CLinical Research Office at Ponce Health Sciences Foundation/Ponce Research I...Dr. Roberto Torres
The Clinical Research Office at PHSU. Innovating Research and Clinical Trials in Puerto Rico. Learn about our capabilities, Moffitt Cancer Center Collaboration, and the Puerto Rico Clinical Trials Network.
Well-trained clinical research professionals are in high demand. The tremendous increase in medical technology and information in the last decade has resulted in an explosion of potential new drugs, devices and biologics that must be tested before being released for use by the public. The profession is constantly challenged to improve and streamline the clinical research programs in order to shorten the development timelines and control the cost for new product development
R&D Directions Webcast June Final[1]cmowen0206
Review a webcast presentation from experts from Vince and Associates Clinical Research, MidLands IRB, and Kendle for three presentations that delve into various aspects of clinical trial patient recruitment, from the perspectives of two prominent CROs and an AAHRPP-accredited independent review board. The presentations for this webinar are:
Phase I Patient Population Trials: Feasibility, Recruitment and Long-term Confinement
Speaker: Dr. Bradley Vince, D.O., Vince and Associates Clinical Research
Beyond Paper: Using Data-Driven Expertise to Enhance Patient Recruitment
Speaker: Jeffrey M. Zucker, Senior Director and Global Head, Patient Recruitment, Kendle
IRB Considerations in Proof-of-Concept Trials
Speaker: Kathy Chase, Pharm.D., IRB chair, MidLands IRB; Director, Provider Services, Cardinal Health - Pharmacy Solutions
R&D Directions Webcast June Final[1]cmowen0206
Review webcast presentation from MidLands IRB, Vince and Associates Clinical Research, and Kendle for three presentations that delve into various aspects of clinical trial patient recruitment, from the perspectives of two prominent CROs and an AAHRPP-accredited independent review board. The presentations for this webinar are:
IRB Considerations in Proof-of-Concept Trials
Speaker: Kathy Chase, Pharm.D., IRB chair, MidLands IRB; Director, Provider Services, Cardinal Health - Pharmacy Solutions
Phase I Patient Population Trials: Feasibility, Recruitment and Long-term Confinement
Speaker: Dr. Bradley Vince, D.O., Vince and Associates Clinical Research
Beyond Paper: Using Data-Driven Expertise to Enhance Patient Recruitment
Speaker: Jeffrey M. Zucker, Senior Director and Global Head, Patient Recruitment, Kendle
Specialized oncology reference laboratory providing the latest testing technologies, global/tech-only options, and interactive education to the pathology community
Offer the complete spectrum of diagnostic services through nationwide network of laboratories
Dedicated to providing superior service, faster turn-around times, and complete attention to the needs of our clients and their patients
Business Valuation Principles for EntrepreneursBen Wann
This insightful presentation is designed to equip entrepreneurs with the essential knowledge and tools needed to accurately value their businesses. Understanding business valuation is crucial for making informed decisions, whether you're seeking investment, planning to sell, or simply want to gauge your company's worth.
Discover the innovative and creative projects that highlight my journey throu...dylandmeas
Discover the innovative and creative projects that highlight my journey through Full Sail University. Below, you’ll find a collection of my work showcasing my skills and expertise in digital marketing, event planning, and media production.
Digital Transformation and IT Strategy Toolkit and TemplatesAurelien Domont, MBA
This Digital Transformation and IT Strategy Toolkit was created by ex-McKinsey, Deloitte and BCG Management Consultants, after more than 5,000 hours of work. It is considered the world's best & most comprehensive Digital Transformation and IT Strategy Toolkit. It includes all the Frameworks, Best Practices & Templates required to successfully undertake the Digital Transformation of your organization and define a robust IT Strategy.
Editable Toolkit to help you reuse our content: 700 Powerpoint slides | 35 Excel sheets | 84 minutes of Video training
This PowerPoint presentation is only a small preview of our Toolkits. For more details, visit www.domontconsulting.com
"𝑩𝑬𝑮𝑼𝑵 𝑾𝑰𝑻𝑯 𝑻𝑱 𝑰𝑺 𝑯𝑨𝑳𝑭 𝑫𝑶𝑵𝑬"
𝐓𝐉 𝐂𝐨𝐦𝐬 (𝐓𝐉 𝐂𝐨𝐦𝐦𝐮𝐧𝐢𝐜𝐚𝐭𝐢𝐨𝐧𝐬) is a professional event agency that includes experts in the event-organizing market in Vietnam, Korea, and ASEAN countries. We provide unlimited types of events from Music concerts, Fan meetings, and Culture festivals to Corporate events, Internal company events, Golf tournaments, MICE events, and Exhibitions.
𝐓𝐉 𝐂𝐨𝐦𝐬 provides unlimited package services including such as Event organizing, Event planning, Event production, Manpower, PR marketing, Design 2D/3D, VIP protocols, Interpreter agency, etc.
Sports events - Golf competitions/billiards competitions/company sports events: dynamic and challenging
⭐ 𝐅𝐞𝐚𝐭𝐮𝐫𝐞𝐝 𝐩𝐫𝐨𝐣𝐞𝐜𝐭𝐬:
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➢CHILDREN ART EXHIBITION 2024: BEYOND BARRIERS
➢ WOW K-Music Festival 2023
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➢ Super Show 9 in HCM with Super Junior
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➢ Korean Vietnam Partnership - Fair with LG
➢ Korean President visits Samsung Electronics R&D Center
➢ Vietnam Food Expo with Lotte Wellfood
"𝐄𝐯𝐞𝐫𝐲 𝐞𝐯𝐞𝐧𝐭 𝐢𝐬 𝐚 𝐬𝐭𝐨𝐫𝐲, 𝐚 𝐬𝐩𝐞𝐜𝐢𝐚𝐥 𝐣𝐨𝐮𝐫𝐧𝐞𝐲. 𝐖𝐞 𝐚𝐥𝐰𝐚𝐲𝐬 𝐛𝐞𝐥𝐢𝐞𝐯𝐞 𝐭𝐡𝐚𝐭 𝐬𝐡𝐨𝐫𝐭𝐥𝐲 𝐲𝐨𝐮 𝐰𝐢𝐥𝐥 𝐛𝐞 𝐚 𝐩𝐚𝐫𝐭 𝐨𝐟 𝐨𝐮𝐫 𝐬𝐭𝐨𝐫𝐢𝐞𝐬."
VAT Registration Outlined In UAE: Benefits and Requirementsuae taxgpt
Vat Registration is a legal obligation for businesses meeting the threshold requirement, helping companies avoid fines and ramifications. Contact now!
https://viralsocialtrends.com/vat-registration-outlined-in-uae/
LA HUG - Video Testimonials with Chynna Morgan - June 2024Lital Barkan
Have you ever heard that user-generated content or video testimonials can take your brand to the next level? We will explore how you can effectively use video testimonials to leverage and boost your sales, content strategy, and increase your CRM data.🤯
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Improving profitability for small businessBen Wann
In this comprehensive presentation, we will explore strategies and practical tips for enhancing profitability in small businesses. Tailored to meet the unique challenges faced by small enterprises, this session covers various aspects that directly impact the bottom line. Attendees will learn how to optimize operational efficiency, manage expenses, and increase revenue through innovative marketing and customer engagement techniques.
The world of search engine optimization (SEO) is buzzing with discussions after Google confirmed that around 2,500 leaked internal documents related to its Search feature are indeed authentic. The revelation has sparked significant concerns within the SEO community. The leaked documents were initially reported by SEO experts Rand Fishkin and Mike King, igniting widespread analysis and discourse. For More Info:- https://news.arihantwebtech.com/search-disrupted-googles-leaked-documents-rock-the-seo-world/
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Activa Cro Presentacion Jan 09
1.
2. Company
Activa is a full-service Contract Research Organization
(CRO) based in Buenos Aires, Argentina
• Established in 2003 in Argentina
• Economic growth rates doubling yearly
• Operating in Chile since 2004
• First spanish Latam CRO Certified ISO
9001: 2000 (2006)
• Operating in Uruguay since 2007
• Established in Mexico in 2008
3. A local CRO with regional reach
México
Chile
Uruguay
Argentina
4. Vision
Through the principles of scientific excellence, flexibility
and adaptability , our aim is to evolve into a “boutique”
CRO, offering specialized services to our clients
Mission
Our endeavour is to satisfy our client requirements and
expectations , working very close to them, in order to
facilitate an efficient management of their projects.
5. Activa was founded and is managed by senior professionals in
Pharmaceutical, Medical device development and Regulatory affairs
We offer combined decades of experience developing basic & clinical research
programs
6. Our aim is to be the leading Regional spanish speaking
CRO in Latin America
Our strenght lies in local and regional expertise, continous training of our
staff and a robust Quality Assurance program
7. Organizational Chart
Board of
Directors
Regulatory Quality Mgnt. Business Administration
Legal External Clinical Trial
Affairs System Development & HHRR
Advisor Auditors Department
Department Department Department Department
Pharmaco- Quality Mgnt.
Project Quality Outsourcing Logistic & Administration
System HHRR
Managers vigilance Assurance Services Supply Chain & Finance
Auditor
Clinical
Research
Associates
8. Organizational Chart
Activa-CRO Headquarters Argentina - January 2009
CTM/CRAs Full Time, Biol, MD,s 13
CRA/CRA ass outsourced to Big Pharma 8
Consultants, MDs 17
Regulatory & QA 4
Business Development 3
Administration 5
Activa-CRO Chile 3
Activa-CRO Uruguay 2
Activa-CRO Mexico 4
9. Our services
Clinical research
Our Scientific Advisory Committee (17 members at this time)
with key investigators and opinion leaders , enables us to
design studies for a wide range of therapeutic areas.
Clinical Research services include:
• Extensive PI Database
• Patient identification, recruitment and retention
• Investigator meeting organization and conduction
• Monitoring Services.
• Site Management.
• Project Management
10. Our services
Clinical research (cont)
• Study Design
• Protocol/CRF Development
• Local Project Coordination (includes sponsor representation for MOH
& customs, contacts with PI, sites and vendors
• Monitor Training
• Supplies warehousing
11. Our services
Regulatory affairs
• Advice on Regulatory procedures in countries of operation
• Site Regulatory Files management
• Ethics committee submissions
• Management of IRB documents and operations
• Local and Regional Regulatory Agency approvals
• Import /Export licenses
• Custom consultancy and management
Our services include the preparation and submission of
registration dossiers. We can recommend modifications in
protocols in order to optimize the registration dossier, including
evaluation of existing data.
12. Our services
Pharmacovigilance Local Representation
• Receiving/Processing/Archiving adverse events in countries of
operation
• Ethics committee /IRB & MOH submissions
• Ensure compliance with local & International requirements
13. Our services
Quality assurance
In December 2006, ACTIVA was granted the ISO 9001:2000
Standard Quality Certification on “Control and surveillance on
clinical research trial processes for the development of drugs,
biological products and medical devices” This certification was
issued by Bureau Veritas Certification and accredited by UKAS
(Europe), ANAB (North America) and OAA (South America).
Activa is the first regional CRO certificated in Management and
Monitoring of Clinical Trials by ISO 9001:2000.
14. Our services
Training
We offer in house training courses designed for clinical research
personnel. Through our associated "Clinical Research Training
Program" with academia (UBA, Fundación Margullies,etc) we
train investigators, monitors, study coordinators and regulators
with focus in the following areas:
• GCP-ICH for investigators
• Monitoring by therapeutic area
• Individual Training Programs
16. Advanced Development Overall Experience December 2003- Jan. 2009
Total No of Studies/Projects 36
No. of Studies/Projects Completed 16
No. of Studies/Projects Ongoing 20
No. of Studies/Projects in Start Up Phase 8
No. of Studies Projects currently active 12
No. of Active Sites 100+
No. of Patients 1000 +
Phases of Studies/Projects Pre-Clinical to Phase IV
Geographical Location of Clients USA/Germany/Switzerland/Spain/Israel
/South Korea/Argentina
Regulatory authorities to whom data is to ANMAT/FDA/EMEA/South Korea
be submitted ANVISA/MOH Uruguay/Mexico/Chile
No. of Therapeutic Areas 11
Agents on which studies being conducted Drugs/Biologics/Devices
Type of Clients Small & Medium Biotech
Small & Big Pharma
Devices Industry
17. Our key factors for success
• We recognize the need for shortened R&D cycles and reduced
costs for testing new products.
• We contact only distinguished and experienced clinical
investigators with combined experience and extensive databases
for patient enrollment.
• Directors have had hands on experience in all aspects of
clinical development
• Our experienced staff is focused on patient safety , strictly
following ICH-GCP standards.
18. Why Latinamerica?
Population: Health System:
• Concentration of medical care in big cities
• Large patient population in almost all type of
• Public, Private, Community and Union
therapeutic indications Hospitals
• Treatment of native patients with similar • Modern central laboratory/imaging centers
ethnic characteristics • High level in telecommunications
infrastructure
• Excellent patient motivation
Sites:
• Experienced Investigators • Established, qualified investigators
Regulatory: • Motivated and enthusiastic investigators
• Well established regulatory environments • Accelerated patient recruitment rates
• Investigators with excellent retention of
• Acceptable regulatory approval timelines patients
• 100% GCP-ICH compliance • High quality data
Market: • Reduced operational costs
Geographical-Cultural:
• Fewer competitive studies
• Inversion of seasons
• Potential commercial market for new • Similar time zones as the United States
products • Prevalent European immigration
• Understanding of English is prevalent