Contract Laboratory .com analytical chemistry, pharmaceutical, toxicology, clinical research, pharmacology, bioanalytical, sterility, pyrogen, medical devices, cosmetics, food, nutritional, preclinical, biomechanical, biotechnology, pharmacokinetic testing laboratories for all your US FDA required GMP, GLP, GCP QC, NF USP, BP, ISO, ANSI, AAMI, AOAC, BAM,  raw material, in-process, and finished product,  testing.
Contract Laboratory .com
Find FDA GMP, GLP, GCP, ISO, CLIA, UKAS, AAALAC, A2LA, and Other Laboratories for All your Laboratory Testing and Scientific Research!
Contract Clinical .com
clinical directories clinical events clinical resources
Account Control Panel

You are not logged in.

Clinical Trial Requests
Clinical Trial Directories
Contract Clinical.com Registration
/td>
2008 Clinical Requests View Current Clinical Requests

Contract Clinical has received the following incoming Clinical Requests which need to be fulfilled ! These Clinical Requests are received from a variety of Pharmaceutical, Medical Device and Biotechnology Companies ranging from start-up companies to large, multinational corporations to government agencies. All are actively seeking Contract Research Organizations and other Clinical Service Providers to perform their Clinical Research, Clinical Trials or provide Clinical Support Services. If you have questions, please call 403-770-1992 or e-mail us. View Current Clinical Requests

Incoming Clinical Requests
#
Therapeutic Area
Clinical Request Description
status
08-0011 Oncology USA Clinical Site Management Organization and Patient Recruitment of normal controls. Protocol requires brief medical history and physical exam and phlebotomy. Samples to be processed at a local lab in addition to samples that must be frozen (-20) and shipped to a central location. ( read more )..... Closed
08-0010 Oncology GCP Clinical Investigators (Medical Doctor and 2 Clinical Research Associates) needed in Belgium for Clinical Study on Oncology Food Supplement. Pre-clinical research has been done (in vitro, in vivo, mechanism of action [depletion of ATP], and toxicity). It is possible to purify and standardize the product, using SFE, BSLT, and HPLC. We are looking for for an MD and two CRA's who have the curiousity and the courage to write a protocol for a Phase I-equivalent clinical trial (20 stage 3 and stag ( read more )..... Closed
08-0009 Dermatology FDA GCP Cosmetics Contract clinical, contract research organization needed for clinical research on Breast Firming Product. ( read more )..... Closed
08-0008 Oncology India Medical Research Institute needs Clinical Trial Consultant for Clinical Research Coordination, Clinical Documentation, Medical Writing ( read more )..... Closed
08-0007 Cardiology Canada Research Institute nees Clinical Trial Project Manager experienced with FDA GCP Clinical Studies needed to manage a GCP study ( read more )..... Closed
08-0006 Dermatology Switzerland Cosmetics Manufacturer needs USA Contract Research Organization to conduct Clinical Study on cosmetic ( read more )..... Closed
08-0005 Nutrition USA Principal Investigator currently doing pharmaceutical clinical trials looking for clinical consultant to assist in diversifing my investigative site into nutraceutical clinical trials ( read more )..... Closed
08-0004 Nephrology Full service FDA, GCP, Part 11 Compliant, ICH Contract Research Organization needed for small Biopharmaceutical Research Company specializing in monoclonal antibodies and research in the area of nephrology and kidney transplant. ( read more )..... Closed
08-0003 Neurology FDA GLP Contract Research Organization needed for conducting Phase I-IIa Clinical Studies on a new pharmaceutical for spinal cord injuries (SCI) to demonstrate safety, tolerability profile and preliminary efficacy in SCI patients. Strong evidence of efficacy has been demonstrated on animal studies. ( read more )..... Closed
08-0002 Pharmaceuticals USA FDA GCP Contract Research Organization needed for Phase III Clinical Trial Study on a Pharmaceutical for BPH treatment. One previous Phase III Clinical Trial Study included an Institutional Review Board APproval but was fairly small. Now a well controlled Clinical Trial Study needs to be done to have adequate documentation for FDA submission as an NDA. ( read more )..... Closed
This information is provided as a service only. Company and product information is prepared by individual companies and has not been independently verified. As such ContractClinical.com can not be responsible for any loss or damage arising from the purchase, sale or use of any service or product through this site.

This site is owned and managed by ContractClinical.com