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October 26, 2023
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  Transforming CDMO Partnerships through a Holistic Understanding of Quality

In pharmaceutical manufacturing, a commitment to quality is fundamental to accelerating time to market, minimizing risk, increasing ROI, and developing life-saving medicines.

However, quality is often mischaracterized by assigning responsibility to a single team, describing it as an end-of-the-line activity, or conflating it with compliance.

While each of these factors is relevant, none defines it. Our whitepaper analyzes the key indicators of a CDMO quality mindset that permeates every aspect of drug development.


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» Industry News
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  Active Pharmaceutical Ingredients Market To Reach USD 346.4 Billion By 2032
According to DataHorizzon Research, the Active Pharmaceutical Ingredients (API) Market size was ... read more »
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  Andelyn Biosciences and Purespring Therapeutics Partner to Manufacture Novel Gene Therapies for Kidney Diseases
Andelyn Biosciences, Inc., a cell and gene therapy Contract Development and Manufacturing ... read more »
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  Aldena Therapeutics Selects PCI Pharma Services to Manufacture Dermatological Disease Treatments
Aldena Therapeutics, a private biotech company pioneering siRNA- based therapies for dermatological ... read more »
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  Avid Bioservices Completes Construction of Cell and Gene Therapy Development and Manufacturing Facility
Avid Bioservices, Inc. , a biologics contract development and manufacturing organization (CDMO) ... read more »

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» Featured Articles
EVENT   In-Flight Data Control: Key to Efficient Life Sciences Business Processes
As pharma companies work on creating a continuous, reliable, harmonized data flow across their ... read more »
EVENT   Most Significant Risk Factors for Emerging and Mid-Market Biopharma Companies - Costly Clinical Trial Delays
In 1820, a group of physicians, driven by concerns regarding the quality and reliability of ... read more »
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» Featured Video
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  Documentary: Cell & Gene Therapy: Advancing the Next Generation of Pharmaceuticals
In this documentary, American Pharmaceutical Review and Pharmaceutical Outsourcing magazine spoke with industry experts to learn how cell and gene therapies are changing the healthcare landscape and ... read more »
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  On-Demand Webinar: Keys to a Successful Tech Transfer for Topical Pharmaceuticals
When looking to do a technical transfer of your drug product, it’s important to understand the steps needed to create and follow an effective and efficient technical transfer process. We will discuss ... read more »

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» Featured White Papers
EVENT   Whitepaper: Addressing Challenges with Clinical In-Use Testing of Biotherapeutics
Lonza Drug Product expert Léa Sorret PhD explores Clinical In-Use Testing of Biotherapeutics in this white paper. Lea shares her expertise and ... read more »
EVENT   Unlocking Clinical Trial Success: Strategies to Boost Enrollment and Enhance Participant Engagement
This infographic gives tips on how to increase quality clinical trial participant enrollments, as well as what to look for in a participant management... read more »
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» More Services
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» Service Directory
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Pharmaceutical Dosage Form Testing and Processing Systems Search More
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| Events
EVENT
  Pharmacovigilance World 2023
London, United Kingdom –  11/01/2023
The Pharmacovigilance World 2023 will provide a platform for the participants to discuss, share and stay updated with present state of affairs in ...
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EVENT
  Bio-IT World Conference & Expo Europe
London, England –  11/29/2023
Bio-IT World Conference & Expo Europe unites a community of leading life sciences, pharmaceutical, clinical, healthcare, informatics, and technology ...
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