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How to Identify Branded Drugs with a Low Likelihood of Generic Entry as Targets for In-Licensing

Drug Patent Watch

It allows us to make more informed decisions and identify opportunities that may have been overlooked using traditional methods.” Conducting Due Diligence Once potential targets are identified, thorough due diligence is crucial to validate the assessment and make informed in-licensing decisions.

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Automation to guide technology shift in aseptic environments

European Pharmaceutical Review

Recently, the European Medicines Agency (EMA) took the lead in pushing for process improvements using technologies already established in other manufacturing sectors. Continuous manufacturing in the biopharmaceutical industry guarantees high quality and high process efficiency.

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These 6 ChatGPT Pharmacy Applications will change your life

pharmacy mentor

Establishing trust in the technology requires: Validating the information provided by ChatGPT: Pharmacy owners can cross-check the information generated by ChatGPT with reliable sources, such as regulatory guidelines, drug databases, or educational materials.

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Pharma News: Latest Trends and Insights for Marketing Teams

Pharma Marketing Network

Table of Contents Sr# Headings 1 Introduction: Why Staying Updated on Pharma News Matters 2 Emerging Trends in Pharma Marketing 3 The Role of Technology in Modern Pharma Strategies 4 Adapting to Regulatory Changes and Compliance Introduction: Why Staying Updated on Pharma News Matters In the fast-paced pharmaceutical industry, information is power.

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Harnessing continuous improvement in the CAPA process

European Pharmaceutical Review

With the corrective and preventive action (CAPA) process often a “one-size-fits-all” approach, a whitepaper by the Medical Device Innovation Consortium (MDIC) Case for Quality Collaborative Community (CfQcc) has instead shared a risk-based framework focusing on continuous improvement. These results are included in most recent paper.

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How to develop GMP compliant software for quality management

GMPSOP

They must follow stringent procedures to validate and maintain their information management systems for GMP compliance.For example, companies located in the USA must comply with the USFDA 21 CFR part 11 regulations. It can also directly contribute to improving the overall quality of products and services and expediting regulatory compliance.

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Balancing cost and value with TCO

Express Pharma

Regular audits, both internal and external, can help identify areas for improvement and ensure continuous compliance. Harnessing the power of data: By leveraging big data and advanced analytics, pharma companies can gain insights into their operations, identify inefficiencies, and make informed decisions to improve performance.