Pharma Compliance and Regulatory Experts
Working with you to achieve your goals
Nassar Consulting is dedicated to helping the Pharmaceutical, Biotech and Medical Device Industry achieve and maintain regulatory compliance and approvals throughout the life cycle of the product from plant design through API sourcing, approval and marketing authorization and post marketing commitments.
Nassar Consulting has international experience encompassing the USA, Europe, the Middle East and the Asia Pacific Region.
Regulatory Consulting throughout drug development cycle (FDA/EU/TGA/MENA)
Compliance Consulting and Auditing (internal/ third party; API and contract manufacturers; sterile and non-sterile) according to FDA and PIC/s guidelines
Non- clinical and Clinical Compliance Consulting and Auditing (GLP/GCP)