Innovating Health for a Better Tomorrow
FA Pharma is one of the leading pharmaceutical consulting company providing pharmaceutical regulatory affairs services to small, medium and large pharmaceutical industries and working throughout the pharmaceutical development, submission, approval and post approval product lifecycle.
FA Pharma consulting has over 20 years of experience in Regulatory Post Approval and Initial Marketing Authorization Application (MAA/BLA), Chemistry Manufacture and Control (CMC) and Global Regulatory Affairs for commercial and developing products, Biological Products, Rare diseases, Vaccines, Large Molecules and Small molecules.
Extensive experience in the writing, reviewing Module 3 and Module 2.3 (QOS) for several commercial and developed products also have experience in pharmaceutical development, manufacturing, analytical development, quality control and quality assurance.
Our tailored solutions help our clients to obtain regulatory approvals fast from health authorities so that the medicinal products available to patients.
We help pharmaceutical companies to register the products and gain regulatory approvals worldwide.
US FDA
PMDA
HA
ANVISA
EMA
KSA
UAE
ANVISA
Qlife Pharma Helps pharma companies to distribute and supply the medicinal products across gulf region
Africa
Brazil
China
Japan
Russia
USA
UK
Europe
4th Floor, 1 Centenary Way, Manchester, M50 1RF, United Kingdom
Phone: +44 1615042500 | Mobile: +447587570977
Email: admin@fapharma.co.uk