Types of Vigilance in Life Sciences

 


In the global life sciences industry, whether you’re launching a new pharmaceutical, a medical device, or a personal care product, the responsibility doesn’t end at regulatory approval. It extends across the product lifecycle, driven by a commitment to patient and consumer safety, and reinforced by an evolving web of global regulatory requirements.

Traditionally associated with large pharmaceutical corporations, vigilance is now a critical function for biotechs, MedTech innovators, cosmetic brands, and emerging-market players alike.

But here’s the challenge: vigilance isn’t one-size-fits-all. Different product categories demand different vigilance systems, each with its own definitions, rules, timelines, and reporting structures.

Let’s explore the three foundational types of vigilance that every regulatory, safety, and quality professional must understand and master.

What is Vigilance in Life Sciences?

At its core, vigilance is the continuous process of monitoring, detecting, evaluating, and reporting undesirable effects or risks associated with healthcare or consumer products. It serves as a feedback loop between real-world use and product safety, enabling manufacturers and regulators to protect public health. Each type of vigilance is tailored to a product category:

  • Pharmacovigilance for drugs and vaccines
  • Materiovigilance for medical devices
  • Cosmetovigilance for personal care and cosmetic products

Understanding the scope and structure of each is critical for compliant and safe market operations.

Read more about types of Vigilance here: Types of Vigilance Every Life Sciences Professional Should Know — DDReg pharma

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