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21/5 Akadeemia tee , Tallinn, Harju maakond, 12618, EE
J. Molner, HQ in Estonia is a comprehensive generic CDRO with experience in topical, liquid, and sterile dosage forms. We offer specialized programs to support IVRT and IVPT for semi-solid bioequivalence as well as Post Approval Change Management of existing or shelved applications. We are EU-GMP release capable and have an MRA with the FDA.
An integrated approach to topical drug development aims to save customers time and cost.
By: Charlie Sternberg
A Q&A with Lucy Zhao, manager of the Skin Lab at CPL discusses the importance of in-vitro Release Testing and how it supports topical drug development.
Released By CPL
Regulatory considerations around bioequivalence in topical generic drug product development.
By: charles evans, marc brown
Stand-alone service offers analytical services including method development, method validation, and stability program design and implementation
By: Kristin Brooks
Adds commercial capabilities and will expand current capacity by 400%
By: Tim Wright
Global pharmaceutical companies outsource topical products to the growing CDMO
The future of topical bioequivalence studies.
By: Theo Kapanadze
novel approach to qualify acyclovir cream products for biowaiver status, potentially replacing clinical trials
Spurred by many factors, global analytical testing services market is experiencing rapid growth in the range of 11% per year
Supports growth of skin permeation/penetration and testing services
Expands services in dermatology development
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