Helping improve the success probability,
one pharmaceutical product at a time.
Take advantage of our global, real-world experience.
Bio Pharma FZC has extensive experience in providing regulatory, product development and quality systems consulting services to developers and manufacturers of pharmaceutical products. Our team of world-class consultants brings decades of experience at every stage of the pharmaceutical regulatory and product development process.
This includes expertise in each of the following elements of the product development process:
- FDA Submissions and Interactions
- Quality Management
- Product Manufacturing
- Medical Device Biocompatibility
- Clinical Trial Design and Evaluation
- GMP, GLP and GCP Regulatory Compliance
- U.S. Agent Services
BIO PHARMA FZC
Office N° 76-C, 1st Floor
Company Reg. N° 13212
Tel: 9716-5263222 – Fax 9716-5263322
Email: contact@ biopharma-fzc.com