Product Development
Formulation Development
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Expertise in a wide range of dosage forms
Designs formulations for targeted delivery of a therapeutic and develops GMP manufacturing processes to ensure a high quality product is produced for clinical trials.
We develop finished products supporting IND, NDA filings and generic ANDA filings. Our facilities have been designed for flexibility, as we offer a variety of dosage forms and the ability to handle highly potent compounds and DEA-controlled substances.
Fact: We have worked with 400+ clients, supporting 400+ compounds and 700+ GMP batches.
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[Webinar] Sterile Nanoemulsion Product Development: Challenges and Future Prospects
Hear a Frontage case study, learn about a nanoemulsion development process using a microfluidizer, and find out what factors to consider while developing a sterile ophthalmic nanoemulsion formulation.
- IND: Formulation development and CTM manufacturing of oral solid, semi-solid (topical), liquid, and sterile dosage forms
- ANDA: Reverse engineering, formulation development, and tech transfer
- Consumer products: OTC reformulation
- High potency suite for CTM manufacturing
- Sterile suite for CTM manufacturing (Phase I)
- DEA manufacturing license for controlled substances (CI-V)
- Proof of Concept studies in animals
- Integrated services with Frontage’s clinical center
Read our article on the development of nanoemulsions and their use as drug-delivery systems.
Resources To Consider
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Sterile Nanoemulsion Product Development: Challenges and Future…
![IVRT Insights From Frontage CMC Experts](https://www.frontagelab.com/wp-content/uploads/2020/03/frontage-image-34434.jpg)
IVRT Insights From Frontage CMC Experts
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CMC-Product Development Services
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