Certification News

EU/UK trade deal fell way short of UK’s initial expectations for medicinal products ahead of negotiations, says Peter Gough at NSF International

Need clarity on determining your QA from your QbD and your cGMPs? You’re not alone! In our new Pharma Explained series from CPhI, we bring you clear cut definitions from industry experts on a myriad of Pharma Terms, delivered in bitesize video presenta...

Excellence in Pharma recognised at virtual ceremony taking place at the CPhI Festival of Pharma.

Inspection conducted remotely using video-conferencing and an online private document sharing platform.

SeaGel offers drug and dietary supplement manufacturers an animal-free and sustainable alternative to traditional soft capsules.

The licence will allow the company to perform EU clinical release for its European customers and drug developers.

Company's manufacturing methods and processes reviewed by an independent third-party auditor to ensure the products have the highest-quality ingredients possible.

The European Medicines Agency (EMA) said Monday it will only issue electronically signed and authenticated certificates for human and veterinary medicines in place of printed ones so it can continue to provide the documents during the COVID-19 pandemic...

India’s Lupin Pharmaceuticals warned Monday it could face regulatory sanctions from the US Food and Drug Administration over its Tarapur active pharmaceutical ingredient (API) manufacturing facility.

In 2018, an Accreditation Certificate of Foreign Drug Manufacturer was certified to Heron’s manufacturing base by Japan Pharmaceutical and Medical Devices Agency (PMDA, No. AG10500666).

Fermenta Biotech Ltd has cleared the required qualification criteria to become Great Place to Work-Certified.