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Understanding WHO Guidelines for Batch Manufacturing Records

Dot Compliance

The World Health Organization (WHO) has established guidelines for BMRs to ensure consistency, quality, and safety across the global pharmaceutical industry. The Importance of Adhering to WHO Guidelines Adherence to WHO guidelines for BMRs is essential for ensuring the quality, safety, and efficacy of pharmaceutical products.

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Everything You Need to Know about Batch Manufacturing Record (BMR) Reviews

Dot Compliance

These records are essential for ensuring consistency, safety, and compliance in the pharmaceutical industry. Each step in the process plays a role in maintaining compliance and preventing product recalls, making BMR review a vital part of quality assurance.

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Pharma & Influencer Marketing: Can They Coexist Ethically?

HIT Consultant

Mike Szczesny, Owner & VP of EDCO Awards & Specialties Influencer marketing in the pharmaceutical industry is a complex issue with reasonable arguments on multiple sides. Their role extends beyond simple promotion—influencing public opinions, driving awareness, and ultimately facilitating a positive impact on public health.

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The Ultimate Guide to ICH Q10 Pharmaceutical Quality Systems

Dot Compliance

It serves as a comprehensive model for ensuring consistent product quality and compliance with regulatory requirements. We’ll also explore how leveraging ICH Q10 can go beyond compliance to offer a competitive edge in the pharmaceutical industry. What is ICH Q10?

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QMS and the ICH Q10 Pharmaceutical Quality System

Dot Compliance

As a result, pharmaceutical companies of all sizes need quality management systems built to address a slew of unique challenges and regulatory oversight. The key framework for creating a QMS that can handle the demands of the pharmaceutical industry is the International Conference on Harmonisation (ICH) Q10 model.

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SQA Regulatory Surveillance Summary for January and February 2024

SQA

A health professional, in the context of a directed donation, did not create a document stating that, in their medical opinion, the use of sperm or ova would not pose a serious risk to human health and safety. Now the Ministry of Health has published revised regulations in accordance with Annex M of the Drugs and Cosmetics Rules.

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Health Provider News – February 18, 2022

Hall Render

Lawmakers call on Biden to end public health emergency. Only 14% of Hospitals Met Price Transparency Rule Compliance. Outpatient push being felt in architecture industry. 5 recent hospital, health system COO moves. of Public Health website. 8 recent hospital, health system executive resignations.