• SKIP TO CONTENT
  • SKIP NAVIGATION
  • Patient Resources
    • Clinical Trial Listings
    • What is Clinical Research?
    • Volunteering for a Clinical Trial
    • Understanding Informed Consent
    • Useful Resources
    • FDA Approved Drugs
  • Professional Resources
    • Research Center Profiles
    • Market Research
    • Benchmark Reports
    • FDA Approved Drugs
    • Training Guides
    • Books
    • eLearning
    • Events
    • Newsletters
    • White Papers
    • SOPs
  • White Papers
  • Clinical Trial Listings
  • Advertise
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » Calvert Laboratories inks deal with Particle Sciences on early-stage development

Calvert Laboratories inks deal with Particle Sciences on early-stage development

March 18, 2013
CenterWatch Staff

Calvert Laboratories and Particle Sciences, two CROs in the fields of preclinical toxicology and drug product formulation, have joined forces to offer a streamlined solution to expedite preclinical drug development activities. 

This partnership aims to alleviate delay issues by aligning formulation and preclinical experts, enabling them to identify the problem and realize the solution more quickly.  Through this collaboration, Particle Sciences develops a formulation specifically aimed at achieving the desired exposure levels to allow Calvert Labs to seamlessly carry out the testing component of the project.

“Formulation is often one of the most significant challenges our clients’ face.  The sooner we can resolve any issues, the more quickly we can help them advance their program forward,” said Charles B. Spainhour, V.M.D, Ph.D., president and chief scientific officer, Calvert Labs.

Mark Mitchnick, M.D., CEO of Particle Sciences, added, “No single group has the in-depth expertise in both formulation and toxicology needed to tackle this.  Through this combined effort, under a single scope of work, our clients are getting a very valuable service unavailable anywhere else.”

    Upcoming Events

    • 16Oct

      MAGI@home Clinical Research Conference 2023

    • 25Oct

      2023 WCG Patient Forum

    • 26Oct

      FDA in 2024: What to Expect in an Election Year

    Featured Products

    • Surviving an FDA GCP Inspection

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

    • Best Practices for Clinical Trial Site Management

      Best Practices for Clinical Trial Site Management

    Featured Stories

    • Donna Snyder

      New WCG Executive Physician Outlines Goals for Clinical Research

    • Hand Shake at Meeting

      Partnership to Bolster Trials in Low Resource Regions Kicks Off

    • Guidelines-360x240.png

      Major Industry Groups Offer Feedback on ICH’s E6(R3) Guidelines

    • AsktheExpertsBadge-360x240.png

      Ask the Experts: Monitoring

    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
    • About Us
    • Contact Us
    • Privacy Policy
    • Do Not Sell or Share My Data

    Footer Logo

    300 N. Washington St., Suite 200, Falls Church, VA 22046, USA

    Phone 703.538.7600 – Toll free 888.838.5578

    Copyright © 2023. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing