Our team can offer complete guidance, including from a regulatory standpoint, for the development and manufacturing of your pharmaceutical product. We have a comprehensive and full-service operation for clinical trial materials preparation in support of Phase I – III development as well as for commercial scale-up and manufacturing of solid, liquid, semi-solid and parental dosage forms, sterile and non-sterile. Our services are cGMP compliant and include established protocols, efficient documentation practices, and effective QA management. We can be your greatest resource.
Formulation development for new chemical (NCE) and new biological (NBE) entities and generic OTC and Rx.
Optimization of existing formulations.
Process development for specific dosage forms.
Improving delivery of existing dosage forms.
Developing controlled release, sustained release, and complex formulations.
Dedicated suites for the handling of DEA Scheduled Compounds.
Support of clinical-niche
API and commercial manufacturing
LET ADPEN TAKE CARE OF YOUR
AND MANUFACTURING NEEDS
ADPEN Laboratories, Inc.
11757 Central Parkway
Jacksonville, FL 32224 USA
Phone: 1 (904) 645-9169
Fax: (904) 641-8423
ADPEN Laboratories, Inc., 11757 Central Pkwy., Jacksonville, FL 32224, USA. (904) 645-9169 – www.adpen.com