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Regulatory Document Management system, electronic rDMS
Freyr rDMS is an end-to-end electronic Regulatory Document Management system exclusively designed to enable Regulatory groups and...
Pharma Regulatory Services, Submissions, Registrations, Licensing
Pharma Regulatory Services Pharmaceuticals as an industry is rapidly growing across the globe. Being one of the crucial sector of life...
PADER Submissions, eCTD Format, FDA, eCTD Software, PAER
A Periodic Adverse Drug Experience Report (PADER / PAER) is a format in which drug companies should submit post market periodic safety...
Nutraceutical Regulatory Intelligence, Classification, Registration
Nutraceuticals Regulatory Intelligence A nutraceutical product is classified as a dietary supplement in one country and the same product...
Medical Writing Services, Regulatory, Clinical, Medical Writing
Medical Writing is a vital segment of clinical research. It plays a critical role in the development and submission of clinical research...
Medical Devices Regulatory Services, US FDA, Europe, Canada, APAC
Medical Devices Regulatory The Medical Device (MD) industry is one of the biggest in healthcare, and with innovation and rapid...
IDMP Software, ISO IDMP Standards, IDMP Management Software
The European Medicines Agency (EMA) is in the process of implementing the standards developed by the International Organization for...
Global Regulatory Solutions - Xtended Global Presence with Local Expertise
Regulatory experts across 120+ Countries, offering localized Regulatory services for Bio-Pharma, Medical Device, Consumer Healthcare &...
Drug Safety, Pharmacovigilance Services, ICSR, FDA, PSUR
Drug Safety and Pharmacovigilance Amid the periodic evolutions and amendments in safety monitoring regulations, maintaining the safety...
eTMF Management, eTMF software, electronic Trial Master File
Audit & Inspection readiness - The first and foremost aspect every Pharma company / a Contract Research Organization (CRO) should...
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