Shakeeb Ur-Rehman

Regulatory Affairs Practice – Europe

OVERVIEW

FOCUS AREAS

Multiple years in the pharmaceutical industry

Regulatory affairs

Regulatory strategy

Preparation of submissions for variations/label updates

GAP analysis and preparation of amendments

Regulatory Affairs Officer with experience as a pharmacovigilance specialist/Regulatory Advisor in the MHRA, experienced with the regulatory processes in the MHRA with a deep understanding of the regulatory processes in the EU. Possessing a MSc in Drug Discovery and Pharma Management from UCL which demonstrates a deep understanding of drug discovery, development and the global pharmaceutical industry.

Extremely ambitious and driven individual willing to learn and grow in all regulatory areas, always ready to deliver to clients no matter the ask. Possessing experience in the MHRA and experience as a Pharmacovigilance Specialist. Excited for the challenges ahead, with a positive aspect on workload and ready to overcome and adapt to any challenge presented.

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