Bioequivalence Studies
Micro Therapeutic Research Labs (MTRL) is a trusted leader in conducting bioequivalence studies in compliance with international regulatory requirements. With over 1,700 successfully completed BA/BE studies, MTRL has built a strong reputation for accuracy, quality, and reliability.
Our independent quality assurance department ensures every study meets stringent global standards, including US FDA, EMA, ANVISA, and NPRA guidelines.
Backed by a diverse volunteer database of more than 32,000 participants, we specialize in healthy volunteers, special populations, and female volunteers. Our expert volunteer mobilization team guarantees timely study execution, making MTRL a preferred partner for global clinical research.
MTRL can undertake the following studies:
- Single & multiple dose studies.
- Fasting & Fed condition studies.
- Drug-Drug Interaction (DDI).
- Pharmacokinetic interaction studies.
- Pharmacodynamic Studies.
- Food Effect studies.
- Cross over, parallel, partial and fully replicate studies.
- Proof of concept studies.
- Special population studies (postmenopausal & adult female studies and geriatric studies).
- Studies comparing routes of administration.
- Studies comparing immediate and modified release forms.
Capability for Various Delivery Routes & Formulations:
- Oral Dosage Forms
- Tablets and Capsules
- Suspensions
- Buccal, Sublingual, and Lozenges
- Injectables
- IV, IM, SC
- Inhalers
- Transdermal Patches
- Nasal Sprays
- Suppositories
- Ointments & Creams