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Clinical Monitoring research, cytotoxicity research, preclinical research, sterility research, Clinical Research research, Clinical Trials research, Clinical Development research, Clinical Supplies research, pharmaceutical research, food research, product safety research, water research, bioburden research

CRO Clinical Requests

IMAGE SOURCE:CDC PHIL technician putting western blot strips in test tray. Antigens if present will bind to sheet and later be detected.

Submit CRO Clinical Requests
Having trouble finding a CRO to perform your research or simply want to save time in calling multiple contract research organizations (CRO)? Submit a CRO clinical request Form or call us at 1-403-770-1992. If any of these CRO's are interested in your CRO research Request , Contract Clinical .com will provide them with your Contact Information. Or if you prefer to maintain your privacy, Contract Clinical .com will also send you the identity of the contract research organizations (CRO) that are able to perform the research. Often contract research organizations (CRO) are found within 24 - 48 hours.
View CRO Clinical Requests
Along with sending contractclinical.com lists all incoming annonymously CRO Clinical Requests where they will be visible to contract research organizations (CRO) 24/7.
Respond to a CRO clinical request
If contract research organizations (CRO) are interested in performing your test, they contact us to indicate their interest. If you choose to remain confidential, we notify you with the contract research organizations (CRO) contact information. If you wish to provide your contact information, we will then provide it to only the contract research organizations (CRO) that are interested and can perform your CRO research.
10 Most Recent Incoming CRO Clinical Requests
10-000011, Medical Device Company needs Eastern Europe CRO for Clinical Trial Design, Data Review, Phase I, monitoring

10-000010, USA or Switzerland CRO needed for Phase 1b proof-of-concept study in mild/moderate psoriasis. Twelve to 18 patients, treated for 4 weeks with one of two dose strengths of a topical formulation of an experimental drug versus placebo with patients acting as their own control. Safety laboratories, phamacokinetics sampling and possible biopsies required.

10-00009, CRO needed for Double blind testing to establish the efficacy of a scar treatment product.

10-00008, Phase 2 to phase 4 clinical trials (anxiety, MDD, obesity, panic, personality disorders, etc)

10-00007, For EU Registration, GCP CRO needed for efficacy clinical study of known pharmaceutical on endometriosis

10-00006, Easter Europe full-service CRO needed for phase I to IV clinical trials, clinical monitoring, patient recruitment,clinical trial data review, bioequivalence study, pk study

10-00005, CRO needed for challenge studies, Proof of Concept studies where healthy volunteers are infected with weakened strains and then administered the test drug.

10-00004, Europe non-GLP Preclinical Contract Research Organization needed for testing antifungals and antibacterial by vaginal delivery.

10-00003, Continential US Contract Research Organization Phase II Clinical Trial Service Provider needed with own sites (7+ sites) and investigators to supplement existing trial through contract directly with Sponsor. Existing network or consortium should have investigators with family practice, general medicine or urgent care duties and a existing patient base.

10-00002, FDA GLP Contract Research Organization needed for GLP efficacy studies of New Castle Disease vaccine , Inactivated , (poultry vaccine)as per the BP ( Veterinary). Challenge protection study in chicks , in isolator.

Clinical Requests for Proposals

Need to find Contract Research or Clinical Service Providers ? Save time searching and find the Clinical Service and Clinical Supply Providers that meet all your requirements at no charge!

Just use our Clinical Assistant and let us do the searching for you! Simply, Submit Clinical Requests !

Are you a Contract Research Organization CRO or a Clinical Service Provider that provides clinical services such as Clinical Trial Design, Phase I Clinical Trials to Phase IV Clinical Trial Studies, Contract Research, Clinical Trial Management, Clinical Trial Monitoring, Clinical Investigative Site, Institutional Review Boards IRB, Clinical Research, Patient Recruitment, Clinical Data Review, Clinical Management, Clinical Supply, Medical Writing, Clinical Data Management, Regulatory Affairs, Proof of Concept Studies, Document Management, Audits, Regulatory Submissions, Clinical Testing, Clinical Supply, Contract Packaging and Contract Labeling, Clinical Training and Education, Language Translation Services, Clinical GLP, ICH GCP Audits, etc ? Find new business! Register your Contract Research Organizations and Clinical Trial Services Register Clinical Companies !

 

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