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Results for tag: "GCP"

CDISC Mapping 2: ODM, MindMaps and References - Product Thumbnail Image

CDISC Mapping 2: ODM, MindMaps and References

  • Training
  • 90 Minutes
  • Global
Russia: Compliance Processes and Regulations - Product Thumbnail Image

Russia: Compliance Processes and Regulations

  • Training
  • 90 Minutes
  • Russia
Making cGMP Documentation Practical - Product Thumbnail Image

Making cGMP Documentation Practical

  • Training
  • 60 Minutes
  • Global
How to Withstand an FDA Audit of your Facility - Product Thumbnail Image

How to Withstand an FDA Audit of your Facility

  • Training
  • 60 Minutes
  • Global
HPLC Method Development and Validation - Product Thumbnail Image

HPLC Method Development and Validation

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  • 60 Minutes
  • Global
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The GCP market within the context of Pharmaceutical Manufacturing is a highly competitive and rapidly evolving sector. It is a market that is driven by the need for pharmaceutical companies to comply with Good Clinical Practice (GCP) regulations. GCP is a set of international ethical and scientific quality standards for the design, conduct, performance, monitoring, auditing, recording, analysis, and reporting of clinical trials. GCP is a critical component of the drug development process, as it ensures that the data generated from clinical trials is reliable and of high quality. As such, GCP is a key factor in the success of a drug development program. The GCP market is comprised of a variety of companies, including contract research organizations (CROs), clinical trial management systems (CTMS), and software providers. These companies provide services such as clinical trial design, data management, and regulatory compliance. Additionally, there are companies that specialize in providing GCP training and consulting services. Some of the companies in the GCP market include Parexel, ICON, Quintiles, Covance, and PPD. Show Less Read more