Unique Formulation Development Solutions: From Concept to Clinical Success

 

087d79db26f64859b7109889539f0f49.png

 

 

 

 

In the competitive pharmaceutical landscape, formulation development plays a pivotal role in transforming a promising molecule into a safe, effective, and patient-friendly dosage form. At Lannett, we specialize in providing unique formulation development solutions that accelerate drug discovery, optimize performance, and ensure regulatory success.

 

Our integrated approach combines scientific expertise, advanced technology, and deep industry experience to deliver high-quality formulations that meet the most demanding project requirements.

Dosage Forms to Support PK and Toxicology Studies

Every successful development program begins with the right dosage form. Our formulation scientists design and develop dosage forms tailored for pharmacokinetic (PK) and toxicology (tox) studies — ensuring consistent bioavailability, stability, and compatibility with study protocols.
By developing early formulations that mirror the intended clinical dosage, we enable faster transitions from preclinical research to first-in-human trials.

Optimization of Existing Formulations

Whether it’s improving bioavailability, modifying release profiles, or enhancing manufacturability, our experts provide formulation optimization strategies that breathe new life into existing products.
Through scientific reformulation, we address issues such as poor solubility, stability challenges, and variable performance — ensuring each product achieves its full therapeutic potential.

Process Development and Scale-Up

From laboratory bench to commercial production, we focus on process robustness and scalability.
Our team develops and validates manufacturing processes that ensure reproducibility, efficiency, and compliance with cGMP standards.
Using advanced analytical tools and process understanding, we seamlessly guide products through scale-up, technology transfer, and validation phases.

Excipient Compatibility and Dosage Form Design

Choosing the right excipients is critical for drug performance and patient safety. Our scientists conduct comprehensive excipient compatibility studies to ensure chemical stability, optimal release characteristics, and manufacturability.
From tablets and capsules to complex injectables, our dosage form design expertise ensures the final product meets the highest quality standards.

Improved Safety and Efficacy

Safety and efficacy are at the heart of every formulation decision we make.
By leveraging advanced formulation technologies — such as nanoparticle systems, solid dispersions, and controlled-release platforms — we enhance the bioavailability and therapeutic effect of APIs while minimizing side effects.
Our commitment to patient-centric design ensures better outcomes and higher compliance.

Reverse Engineering and Reformulation

Our reverse engineering capabilities enable us to deconstruct and analyze existing market products to improve or reproduce them for generic or differentiated development.
This analytical expertise allows us to benchmark quality attributes, identify formulation opportunities, and create cost-effective, high-performance alternatives.

Partnering for Innovation

From concept to commercialization, our formulation development services are designed to help pharmaceutical partners bring better medicines to market — faster, safer, and more efficiently.
We combine science, innovation, and collaboration to deliver solutions that make a measurable difference in patient care.

Lannett’s unique formulation development solutions empower our partners with the flexibility, quality, and expertise needed to achieve success across every stage of the drug development lifecycle.

Comments

Post a Comment

Popular posts from this blog

Contract Sales in Pharmaceutical Companies: A Strategic Approach

Image
  Pharmaceutical companies face multiple challenges when it comes to launching new drugs and expanding the market for existing ones. One of the primary hurdles is building and maintaining an effective sales force to drive product uptake. Given the highly competitive nature of the pharmaceutical industry and the significant investment required to develop and bring a new drug to market, many companies are turning to  contract sales organizations (CSOs)  for flexible, efficient, and cost-effective sales solutions. In this blog, we will explore what  contract sales in the pharmaceutical industry  entails, its benefits, and how it shapes the future of pharmaceutical marketing. What is Contract Sales? Contract sales refer to the outsourcing of sales functions to specialized third-party organizations known as  Contract Sales Organizations (CSOs) . These companies provide trained sales professionals who work on behalf of pharmaceutical companies to promote, sell, a...
Read more

The growing importance of medicine in the modern world

Image
    Innovation and efficiency are key success factors in the ever-growing pharmaceutical industry. An important external player, often overlooked but critical to management, is the  pharmaceutical contracting organizations  (CMOs) These entities provide essential services that support pharmaceutical companies bring new drugs to market faster, more cost-effectively and with higher quality   What is Pharmaceutical Contract Manufacturing?   Pharmaceutical contracting refers to the outsourcing of drug manufacturing primarily to companies. These CMOs offer a broad range of services from pharmaceutical products to clinical trials, and finally, commercial drug development and CMO collaboration enables pharmaceutical companies to engage their partners manufacturers knowledge and capabilities to focus on their core competencies, such as research and development   The Benefits of Using CMOs One of the primary benefits of working with CMOs is cost-effectiveness. ...
Read more

Empowering Innovation: The Critical Role of Pharmaceutical Contract Manufacturers in the Drug Development Landscape

Image
In the intricate tapestry of the pharmaceutical industry, where precision and quality are paramount, the emergence of pharmaceutical contract manufacturers has significantly reshaped the landscape. These entities, often operating in the background, are integral to the seamless development, production, and distribution of pharmaceutical products. In this exploration, we'll unravel the multifaceted role of pharmaceutical contract manufacturers, shedding light on their significance, benefits, and the key factors that contribute to their success. Understanding Pharmaceutical Contract Manufacturing: Pharmaceutical contract manufacturing is a strategic practice in which pharmaceutical companies outsource the production of drugs and pharmaceutical products to specialized third-party manufacturers. These manufacturers are equipped with state-of-the-art facilities, cutting-edge technology, and a skilled workforce dedicated to the intricacies of pharmaceutical production. The primary objecti...
Read more