Pre-clinical And Clinical Services
FROM BENCH TO CLINIC
At Krescent, we provide independent expert advisory services in pharmacological and non-clinical safety evaluations to the pharmaceutical products, new chemical Entities (NCEs) to assist your drug development program.
Our expertise includes the areas of in vitro and in vivo pharmacology, toxicology, drug metabolism and pharmacokinetics.
We expertise providing inputs on preclinical animal model development and screening of compounds. We provide inputs on study design and new animal model development for screening of pharmaceutical product.
We provide complete preclinical ADME (absorption, distribution, metabolism, excretion), pharmacology, and pharmacokinetic (PK) strategy and implementation services to help your molecule get into the clinic and through development as efficiently as possible.
- Preclinical ADME/PK plan development and implementation
- In vivo and in vitro experiment planning
- Regulatory ADME, pharmacology, and toxicokinetics (TK) report
- Critical review and gap analysis of submissions
We believe that effective decision making will help client to save resources and valuable time in demanding global environment.
We at Krecent have special expertise in:
Contact us to start a conversation with one of our team members about your unique resourcing goals and how we can put you on the path to success.
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Contact
-
B804, Harit shilpa, Rahatani,
Pune-411 017, MH, India - +91-9028293366
- discover@krescentmr.com
Brochures
View our 2022 Clinical prospectus of
brochure for an easy to read guide on
all of the services offer.
