1987 -1996 Director, Regulatory Affairs @ Central Pharmaceuticals
Mark Aikman Education
University of Kentucky
Doctor of Pharmacy (Pharm.D.) (Pharmacy)
Butler University
Mark Aikman Skills
Pharmacology
Continuous Improvement
Startups
Research and Development (R&D)
Quality Assurance
Rare Diseases
Business Development
Project Management
Manufacturing
Pharmacovigilance
Biopharmaceuticals
Oncology
Pharmaceutical Industry
Biotechnology
FDA
Clinical Development
Clinical Research
Clinical Trials
Drug Development
GCP
Regulatory Affairs
Lifesciences
Sop
GMP
GLP
Technology Transfer
Regulatory Submissions
CRO
CTMS
Life Sciences
Standard Operating Procedure (SOP)
Regulatory Requirements
Standard Operating Procedure Sop
Standard Operating Procedure
Mark Aikman Summary
Mark Aikman, based in Wilmington, NC, US, is currently a VP, Regulatory Affairs at Piramal Critical Care. Mark Aikman brings experience from previous roles at Reg-Tec, Inc., Osmotica Pharmaceutical Corp., Steris Laboratories and Schwarz Pharma. Mark Aikman holds a Doctor of Pharmacy (Pharm.D.) in Pharmacy @ University of Kentucky. With a robust skill set that includes Pharmacology, Continuous Improvement, Startups, Research and Development (R&D), Quality Assurance and more. Mark Aikman has 1 emails and 1 mobile phone numbers on RocketReach.
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