Edapt specialises in providing expert support for medical affairs activities ensuring delivery of high quality and compliant scientific services, quality documentation and materials.
We have worked with pharmaceutical and medical device companies, creative agencies and start-ups on a UK, European and Global level.
Our agile approach will help you meet your business and regulatory objectives regardless of your scope of work or size of organisation.
Some of our previous clients include: Merck Serono, Grünenthal, Edwards Life Sciences, Lucid Group, Merz Pharma UK Ltd.
Our team is highly skilled and qualified across multiple therapeutic areas. Expertise includes:
• Compliance Specialists
• AQP/Scientific Advisors
• Medical Information Scientists (including PV expertise)
• Medical Writers
• Training and Development specialists
• GDPR specialists
• QA Specialists
We are members of TOPRA, PIPA, MAAPS, Faculty of Pharmaceutical Medicine
Claire Cherry, the founder of Edapt, has over 25 years of experience in both Pharmaceutical and Medical Devices industries. An experienced Medical Director who has worked in Medical Information, Medical Education, Regulatory Affairs, Quality Assurance and Compliance roles she brings a wealth of experience to the companies she has worked with.
Edapt Ltd was founded in 1997. Our experienced team are here to support medical, quality and compliance functions.
All standards are aligned to:
MHRA (Medicines and Healthcare Regulatory Authority)
ABPI (Association of British Pharmaceutical Industry)
IPHA (Irish Pharmaceutical Healthcare Association)
EFPIA (European Federation of Pharmaceutical Industries and Associations)
ABHI (Association of British HealthTech Industries)
ASA (Advertising Standards Agency) Guidelines
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