Pharmaceutical Manufacturing Facilities Registration in UAE (MOHAP)
In the United Arab Emirates (UAE), the Ministry of Health and Prevention (MOHAP) plays a crucial role in regulating pharmaceutical […]
Pharmaceuticals
Pharmacovigilance System Master File (PSMF)
Pharmacovigilance (PV) is one of the most important parts of the drug product process. PV deals with the detection, assessment
Regulations for Pharmaceutical Registration in Hong Kong
Pharmaceutical market in Hong Kong has reached a significant size, estimated to be around $2.3 billion. This figure highlights the
Pharmacovigilance of Biologics in the USA (US FDA)
Pharmacovigilance plays a vital role in ensuring the safety and efficacy of biologics, which are complex therapeutic agents derived from
US FDA Pharmacovigilance Requirements For Drugs in the USA
Pharmacovigilance is a cornerstone of drug regulation in the USA, playing a crucial role in ensuring the safety and efficacy
MHRA Pharmaceutical Regulations and Registration in the UK
In 2024, the Pharmaceuticals market in the United Kingdom is poised for significant growth, with projected revenue expected to reach
PADER In Pharmacovigilance: How To Prepare?
PADER (Periodic Adverse Drug Experience Report) is one of the critical components of pharmacovigilance. It is a part of the
Pharmaceutical Regulations and Registration in Australia
The pharmaceutical market in Australia is projected to reach USD 9.78 billion by the end of the year 2023 with
Pharmacovigilance In Clinical Trials
Clinical trials are an integral part in the development of medical products. It is done to ensure that the product