Regulatory Affairs Certificate
Issued 08/2021 • Expires 08/2027
Study director specializing in preclinical and clinical pharmacology studies. Experienced in protocol design and regulatory submissions. Expert in bioequivalence study design and execution.
Desired delivery: before 1 Jun 2025
Manufacturer: Singapore Equip Business Analyst Pte. Ltd., Malaysia
Lead time: 21 days
Distributor: Italia Pharma Formulations S.r.l., Cyprus
Lead time: 90 days
Buyer: Italia Pharma Formulations S.r.l., Cyprus
Desired delivery: before 1 Dec 2025