Home » Authors » CenterWatch Staff

Articles by CenterWatch Staff

Regeneron launches new human genetics initiative

January 14, 2014

CenterWatch Staff

Crealta Pharmaceuticals acquires Savient Pharmaceuticals

January 14, 2014

CenterWatch Staff

Quintiles, The Medical Affairs Company collaborate

January 13, 2014

CenterWatch Staff

Qiagen, Exosome Diagnostics to develop diagnostics for cancer

January 13, 2014

CenterWatch Staff

Lexicon reorganizes, cuts 115 R&D jobs

January 13, 2014

CenterWatch Staff

FutuRx begins operations in Israel

January 13, 2014

CenterWatch Staff

goBalto expands internationally

January 13, 2014

CenterWatch Staff

Lilly acquires Arteaus Therapeutics’ CGRP antibody for migraine prevention

January 13, 2014

CenterWatch Staff

CROS NT acquires MDSL International

January 13, 2014

CenterWatch Staff

Jazz Pharmaceuticals acquires Aerial Biopharma’s rights to investigational compound

January 13, 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

Regeneron launches new human genetics initiative

Crealta Pharmaceuticals acquires Savient Pharmaceuticals

Quintiles, The Medical Affairs Company collaborate

Qiagen, Exosome Diagnostics to develop diagnostics for cancer

Lexicon reorganizes, cuts 115 R&D jobs

FutuRx begins operations in Israel

goBalto expands internationally

Lilly acquires Arteaus Therapeutics’ CGRP antibody for migraine prevention

CROS NT acquires MDSL International

Jazz Pharmaceuticals acquires Aerial Biopharma’s rights to investigational compound

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.