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Streamlining Compliance in the Pharmaceutical Industry with the eQMS

Dot Compliance

In the pharmaceutical industry, the importance of regulatory compliance extends beyond fulfilling legal obligations. Compliance can be streamlined with the help of an electronic quality management system (eQMS) that incorporates regulatory standards into every operational aspect of a pharmaceutical organization.

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Best Practices for Conquering Data Management Challenges in the Pharma Industry

HIT Consultant

In addition to regulatory fines triggered by compliance violations, failing to manage data accurately could lead to issues like the sale of expired medications, causing harm to patients. Best practices for managing pharmaceutical data Again, there are no simple solutions for streamlining data management in the pharmaceutical industry.

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Healthy Data Management: How IT Assists Healthcare Institutions

Healthcare IT Today

Confidentiality Laws and regulations govern the confidentiality of medical data. However, it is crucial to consider the compliance of chatbots with security standards. About Natalie Tkachenko Natalie is a HIPAA-certified expert with high-grade knowledge in the healthcare and pharmaceutical industries.

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Healthy Data Management: How IT Assists Healthcare Institutions

HIT Consultant

Confidentiality Laws and regulations govern the confidentiality of medical data. However, it is crucial to consider the compliance of chatbots with security standards. State documents define rules for collecting, storing, processing, and transmitting medical information. Currently, ChatGPT does not meet HIPAA standards.

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How to Tackle Pharma’s 3 Biggest Compliance Risks Head-On with Verisys

Verisys

How to Tackle Pharma’s 3 Biggest Compliance Risks Head-On with Verisys How often have you started at a new organization and heard these phrases? “ Some companies make decisions based on compliance standards and optics, while others may be more lax. Clinical trial compliance can offer unique challenges for pharmaceutical companies.

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SQA Regulatory Surveillance Summary 5 | Monthly Update 2021

SQA

This technical report focuses on the challenges facing the pharmaceutical industry that use complex packaging systems for sterile drugs and biologics (e.g., government agencies and the private sector to collaborate in providing Americans with timely access to pharmaceuticals.

FDA 83
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Monthly Round-Up of What to Read on Pharma Law and Policy 

Bill of Health

The selections feature topics ranging from an analysis of government and industry investments for recently approved drugs, to a discussion of court decisions on mifepristone, and an examination of the added therapeutic benefit associated with the top-selling brand-name drugs in Medicare. JAMA Health Forum. 2023 Apr 7;4(4):e230511.