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About Us

Founded in 2004, Lipont Pharmaceuticals Inc. specializes in the research and development of innovative pharmaceutical solutions. Our headquarters in Richmond, British Columbia, is home to a team of skilled Ph.D. scientists dedicated to making a difference in the generic drug market. We pride ourselves on our commitment to quality, confidentiality, and customized service for each of our esteemed clients.

Our Services

Innovative Drug Development

We specialize in synthesizing and formulating Active Pharmaceutical Ingredients (APIs) with a focus on quality and efficiency.

Process Development and Scale-Up

Our team is dedicated to process optimization to ensure a smooth transition from lab to large-scale manufacturing.

cGMP Manufacturing

We adhere to current Good Manufacturing Practices to ensure high-quality production of pharmaceutical products.

Pre-Formulation and Analytical Development

Our analytical capabilities ensure formulation success through rigorous testing and validation processes.

Pharmaceutical Formulation Development

Tailored formulation development that meets the unique specifications of our clients.

Regulatory Support

We provide comprehensive technical documentation and regulatory support, facilitating smooth product approvals.

FAQs

Lipont specializes in high-quality generic APIs and related intermediates tailored to client specifications.

We follow strict cGMP guidelines and conduct thorough quality control at each stage of production.

Lead times vary based on project scope; our team works diligently to meet client timelines.

Yes, we provide complete technical documentation packages and regulatory support for submissions.

Absolutely, we prioritize client confidentiality and adhere to strict agreements.

Our R&D team consists of Ph.D.-level scientists with over 15 years of industry experience.

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