Supporting the pharmaceutical industry
Medicinal Products
Integrated services specialising in development, regulatory affairs, quality, and pharmacovigilance—expert advice and efficient solutions to support your project towards success.
Our specialist pharmaceutical consultants are all seasoned medicinal product development and compliance experts who offer scientific expertise, specialised knowledge, and experience across all phases of medicinal product development and the intricacies of regulatory compliance (EMA, MHRA, FDA, PMDA) from non-clinical to regulatory approval.
General consulting and Troubleshooting
Strategic and Tactical Product and Device Development
Regulatory Affairs
Pharmacovigilance and Medical Device Vigilance
EU and UK Sponsor Legal Representation
EU and UK GDPR Compliance Services
Our services include:
General consulting and Troubleshooting
Strategic and Tactical Product and Device Development
Regulatory Affairs
Pharmacovigilance and Medical Device Vigilance
EU and UK Sponsor Legal Representation
EU and UK GDPR Compliance Services
We advise the pharmaceutical industry, institutions, researchers, and investors regarding the development, regulatory approval, and postmarketing scientific support across a broad range of therapeutic areas, including:
Cardiology/Vascular
Dermatology
Endocrinology and Metabolism
Gastroenterology
Immunology
Infectious
Musculoskeletal
Nephrology/Urology
CNS/Neurology
Obstetrics and Gynaecology
Oncology
Paediatrics/Neonatology
Pain
Psychiatry
Rare diseases
