2017 FDA Governance World Health 
Bill of Health
JULY 14, 2023
The federal government’s commitment to assuring that participants in human subject research provide fully informed consent dates back to the U.S In 2017, Congress acted again to update the Common Rule and strengthen the provisions related to consent. While the U.S. These warnings echo those of the U.S.
Exeed Regulatory Compliance
MARCH 5, 2020
Secretary of the Department of Health and Human Services (HHS) has declared a public health emergency. The World Health Organization (WHO) has stopped short of classifying the outbreak as a pandemic, but consistently encouraged affected countries to activate their national emergency response plans.
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
SQA
FEBRUARY 15, 2023
A new template for the Certificate of a Pharmaceutical Product will be put into use in line with China’s pharmaceutical export practices and the latest World Health Organization (WHO) guidelines. PCPC looks forward to working with the FDA and key stakeholders to implement this important legislation.
SQA
OCTOBER 18, 2023
The US FDA has already recognized the ability of 16 EU Member States to conduct GMP inspections of manufacturers of veterinary medicinal products. At the same time, the EU has recognized the US FDA as an equivalent authority to carry out these inspections.
SQA
JULY 8, 2022
It is not intended to provide information on the terms and procedures directly associated with regulatory requirements governing cell-based products. World Health Organization (WHO). The guide emphasizes the effect that cryopreservation and recovery may have on cell viability and cell function.
Expert insights. Personalized for you.
130 
Let's personalize your content