Patient Safety and Product Quality
At Insmed, the health and safety of our patients is our top priority, and we work together to ensure the highest levels of quality and safety in our products. We comply with the safety and quality regulations that govern our products and report any product-related concerns if they arise.
How we do it
- We put our patients first in everything we do.
- We train our people to recognize and report an adverse event, complaint, or concern about a product.
- We follow all Insmed procedures and applicable laws that apply to the safety and quality of our products.
- We present information about our products truthfully and accurately at all times and in all materials.
- We prioritize accuracy and completeness in all data that support product safety or efficacy.
- We are transparent in communications with regulatory agencies, HCPs, third-party suppliers, and patients.
Did you know?
Adverse events
Adverse events are any unintended, undesirable, or unexpected occurrence associated with the use of a medical product, regardless of whether it is directly caused by the product. Keep in mind that an adverse event is not always a negative side effect and is not necessarily caused by an Insmed product.
Product complaints
Product complaints are any communication that alleges deficiencies related to the identity, quality, durability, reliability, safety, effectiveness, or performance of a drug or device after it is released for distribution.
You must report an adverse event or product complaint immediately as follows:
Europe
All other countries
Visit insmed.com/med-info for a country-specific list of contacts where you can report an adverse event or submit a product complaint.
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