This site uses cookies to improve your experience. By viewing our content, you are accepting the use of cookies. To help us insure we adhere to various privacy regulations, please select your country/region of residence. If you do not select a country we will assume you are from the United States. View our privacy policy and terms of use.

Remove Food Remove Healthcare Provider Remove Pharmaceutical manufacturing Remove Safety
article thumbnail

Getting ahead of regulatory changes around PFAS in pharmaceutical packaging

Clarivate

MARCH 14, 2024

Over the past few years nitrosamines and nitrosamine impurities have been increasingly gaining the reputation of being high-risk containments in the food industry. The food sector has already initiated the publication of preliminary regulations aimed at restricting PFAS in packaging. [3].

Pharmaceutical 52
Pharmaceutical Manufacturing Food Healthcare Provider 52
article thumbnail

US legislative update: takeaways for European pharma

European Pharmaceutical Review

NOVEMBER 8, 2022

In the US, members of the public can request, through a Citizen Petition, that the US Food and Drug Administration (FDA) “take or refrain from taking” various administrative actions, including denying approval of generic and biosimilar drug applications. Senate Bill 562 (S.

Food and Drug Administration 52
Food and Drug Administration Pharma Prescription Manufacturing 52
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

 

Stay Connected

Join 8,000+ Insiders by signing up for our newsletter

About
About
Editions
Editions
Topics
Powered by Aggregage | Terms and Conditions | Your California Rights and Privacy Policy
© Aggregage 2024