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Belmar Research © ALL RIGHTS RESERVED. 

303-222-5102

cONTACT@bELMARrESEARCH.COM


Belmar Research offers institutions a turnkey solution for clinical drug trials, allowing them to focus on conducting their study without the distraction of managing the supporting processes and activities related to the drug supply chain, packaging and subject tracking




We are a contract manufacturer specializing in
​research support. We are unique in that we are
licensed as both a compounding pharmacy and
a FDA-registered drug manufacturing facility. This
allows us the ability to support the many different
​styles and phases of studies, from small to
large, from individual patient doses to bulk
manufacturing.


Our services include:

​MANUFACTURING

Active ingredient sourcing - We will procure the drug under study in the quantity you need from our network of wholesale suppliers.

Dose Escalation - We can manufacture a specific dose of an approved generic if that dose is not available commercially.

Placebo manufacturing - Our proven manufacturing processes, including advanced embossing, color, and coating capabilities, deliver placebos that are visually identical to the active ingredient being studied.

Dose forms
- We have the ability for production of sublingual and oral tablets, capsules, topicals, creams and powders.

Formulation services - With experienced staff, we will work to find the perfect formulation to fit your needs.

Testing - We offer independent-lab testing services for all products.


DISPENSING

We can deliver study medications to your study in a variety of ways; in bulk to your institutional pharmacy, pre-packaged for future-randomized subjects or packaged specifically for current-randomized subjects.

Tracking of patients - Maintain dispensing records for each specific patient throughout the study.

Inventory control - Ability to dispense and store inventory as required.

Packaging and labeling - We offer the packaging and labeling services you need to ensure compliance with your study guidelines and procedures.

Recording and reporting - All documentation related to the trial will be stored. This includes manufacturing records, patient dispensing, and subject to medication compliance.


​STUDY SUPPORT

Randomized trial and blind study support
- We offer the tracking and monitoring to support a double blind cross-over controlled study, from randomization to subject compliance reporting.

Contact us today to find out how we can support you in conducting a successful clinical trial. 


INSTITUTIONAL RESEARCH SUPPORT