Home » Authors » CenterWatch Staff

Articles by CenterWatch Staff

NIA/NIH grants $1.4M to Cognition Therapeutics' Alzheimer's program

May 23, 2014

CenterWatch Staff

Human Longevity hires for clinical, regulatory/scientific and informatics

May 22, 2014

CenterWatch Staff

Inhibikase Therapeutics receives Orphan Drug Designation for PML

May 22, 2014

CenterWatch Staff

Jack Modell joins Rho as senior medical officer

May 22, 2014

CenterWatch Staff

ImaginAb launches Japanese subsidiary

May 22, 2014

CenterWatch Staff

Clinverse, eClinical Insights partner

May 22, 2014

CenterWatch Staff

Inovio Pharmaceuticals acquires DNA therapies from University of Pennsylvania

May 21, 2014

CenterWatch Staff

Neurotrope, Stanford expand collaboration

May 21, 2014

CenterWatch Staff

SBRI Healthcare launches new competition, $4.2M available to small businesses

May 21, 2014

CenterWatch Staff

PDS launches first publicly available, FDA-validated dataset for SEND

May 21, 2014

CenterWatch Staff

Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials

The information you need to adapt your monitoring plan to changing times.

Learn More Here

Articles by CenterWatch Staff

NIA/NIH grants $1.4M to Cognition Therapeutics' Alzheimer's program

Human Longevity hires for clinical, regulatory/scientific and informatics

Inhibikase Therapeutics receives Orphan Drug Designation for PML

Jack Modell joins Rho as senior medical officer

ImaginAb launches Japanese subsidiary

Clinverse, eClinical Insights partner

Inovio Pharmaceuticals acquires DNA therapies from University of Pennsylvania

Neurotrope, Stanford expand collaboration

SBRI Healthcare launches new competition, $4.2M available to small businesses

PDS launches first publicly available, FDA-validated dataset for SEND

Featured Products

Surviving an FDA GCP Inspection: Resources for Investigators, Sponsors, CROs and IRBs

Best Practices for Clinical Trial Site Management

Featured Stories

Thought Leadership: Remote Patient Monitoring Gives New View of Safety in Cardiac Clinical Trials

Ask the Experts: Applying Quality by Design to Protocols

Clinical Trials Need Greater Representation of Obese Patients, Experts Say

FDA IT Modernization Plan Prioritizes Data-Sharing, AI, Collaboration and More

Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials

The information you need to adapt your monitoring plan to changing times.