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Is the microbiome therapy hype up for a reckoning?

Pharmaceutical Technology

The idea behind these treatments relies on altering the gut microbiome by designing therapeutics that contain bacteria derived from donated stool samples. According to the company’s website, the biotech is undertaking research to decide on the future of the ulcerative colitis program, which also includes another candidate called SER-301.

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Transforming Your Informed Consent Process

Cloudbyz

If you’ve been around the clinical research industry, the concept of obtaining electronic consent is probably familiar to you. A secure solution also provides various methods of document authentication by requiring participants to upload multiple forms of identification such as a state ID, driver’s license, and/or a health card.

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Client-Pharma FAQs During the COVID-19 Crisis

Client Pharma

Response : contain, control or minimize the impacts of any incident(s). Preparedness : take steps before an incident to ensure effective response and recovery. Recovery : take steps to minimize disruption and recovery times. Q: How are Client-Pharma’s warehousing and distribution channels being managed?

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Key Items Auditors Look for When Reviewing an Investigator Site File

Advarra

Maintaining complete and compliant documentation while managing the complex processes and interactions of clinical trial conduct is complicated. Investigator Site Files The ISF contains essential documents permitting evaluation of a clinical trial’s conduct. Both the medical licenses and nurse licenses need to be up to date.

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Client-Pharma FAQs During the COVID-19 Crisis

Client Pharma

Response : contain, control or minimize the impacts of any incident(s). Preparedness : take steps before an incident to ensure effective response and recovery. Recovery : take steps to minimize disruption and recovery times. Q: How are Client-Pharma’s warehousing and distribution channels being managed?

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Pfizer and Valneva Issue Update on Phase 3 Clinical Trial Evaluating Lyme Disease Vaccine Candidate VLA15

Pfizer

GCP is the international ethical and scientific quality standard for clinical trials that all clinical researchers need to follow. The clinical trial remains ongoing with other sites not operated by the third party, and Pfizer continues to enroll new participants at those sites.

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Phase 2 FIGHT Trial Results Presented at ASCO GI Validate Importance of FGFR2b Overexpression and Reinforce Potential of Bemarituzumab Plus Chemotherapy as a Frontline Targeted Treatment for FGFR2b+ Gastric and GEJ Cancers

The Pharma Data

Associate Professor of Medicine at UCLA, Co-director of the Gastrointestinal Oncology Program and Director of Early Phase Clinical Research at the Jonsson Comprehensive Cancer Center. Five Prime collaborates with leading global pharmaceutical companies and has therapies in pre-clinical and clinical development.

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