The quality of trial data depends on a rigorous sample management process that safeguards the integrity of samples at every step, from initial specimen collection through bioanalysis, to post-study storage. A CRO partner that conducts both preclinical and clinical studies, and supporting bioanalysis, ensures continuity of processes, knowledge sharing, and a centralized location for long-term storage of all your samples.

Click here to download a readable, PDF version of Issue 23: https://www.altasciences.com/sites/default/files/2022-05/The_Altascientist_issue-23_Sample-Management_v3.pdf

CHAPTERS:

- 0:16 ― Section 1: Introduction

- 1:41 ― Section 2: Sample Collection and Storage Conditions

- 4:16 ― Section 3: Standardized Workflows for Risk Management and Chain of Custody Maintenance

- 5:54 ― Section 4: Stability Testing

- 7:34 ― Section 5: Laboratory Management

- 8:57 ― Section 6: Customized Processes

- 10:35 ― Section 7: Management of Bioanalytical Matrices

- 11:21 ― Section 8: Post-Study Sample Management

- 12:12 ― Section 9: Conclusion

About Altasciences:

Altasciences is an integrated drug development solution company offering pharmaceutical and biotechnology companies a proven, flexible approach to preclinical and clinical pharmacology studies, including formulation, manufacturing, and analytical services. For over 25 years, Altasciences has been partnering with sponsors to help support educated, faster, and more complete early drug development decisions. Altasciences’ integrated, full-service solutions include preclinical safety testing, clinical pharmacology and proof of concept, bioanalysis, program management, medical writing, biostatistics, clinical monitoring, and data management, all customizable to specific sponsor requirements. Altasciences helps sponsors get better drugs to the people who need them, faster.