For SMEs and biotechs expanding across Europe, scaling pharmacovigilance (PV) isn’t about adding peo...
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Scaling pharmacovigilance (PV) across Europe is as much an organizational challenge as it is a regul...
As pharma and biotech companies expand globally, one of the most underestimated challenges they face...
Pharmacovigilance (PV) is no longer just a regulatory requirement; it has become a strategic busines...
Ensuring the safety of authorised medicines doesn’t happen by accident. It takes a well-structured s...
What do you do when a healthcare professional emails your company about off-label use Or when a pati...
Pharmacovigilance (PV) is vital to public health. According to the Spanish Agency for Medicines and ...
In the fast-paced world of biopharmaceuticals, innovation often means launching new products. But wh...
Vaccines are among the most powerful tools in modern medicine, but monitoring vaccine safety doesn’t...
With people, animals, and ecosystems more connected than ever, safeguarding animal health and veteri...
In the European Union, ensuring the safety of human pharmaceutical products requires strict complian...
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Pharmacovigilance Agreements (PVA), also known as Safety Data Exchange Agreements (SDEA), are essent...
Pharmacovigilance is a cornerstone of patient safety and public health, ensuring that the benefits o...
With rapid advancements in medical technology reshaping healthcare, new devices and innovations are ...
As healthcare and patient safety become more important than ever, pharmaceutical companies are total...
In 2023, assessment timelines for Clinical Trial Authorization (CTA) applications and substantial am...
In the world of pharmaceuticals, ensuring the safety and efficacy of medicines is paramount. One cru...
The safety of medicines is a fundamental concern in the field of public health, and in Europe, pharm...
Did you know millions of patients are already discussing medications and side effects online? Social...
Patient Support Programs (PSPs), as outlined by the Good Pharmacovigilance Practices (GVP) Module VI...
The UK Medicines and Healthcare Products Regulatory Agency (MHRA) has been conducting Good Pharmacov...
In healthcare, safeguarding patient safety and upholding the integrity of pharmaceutical interventio...