Research & Development

Research Formulation

Advancing Science, Delivering Care

At HAB Pharma, Research and Development (R&D) is driven by a clear purpose: to translate pharmaceutical science into safe, effective and patient-focused medicines. Our formulation R&D brings together scientific expertise, rigorous development processes and a deep understanding of drug delivery to create formulations built for quality, stability and consistent performance.

From selecting the right formulation and excipients to optimization, analytical evaluation and stability testing, we follow a structured approach to transforming active pharmaceutical ingredients into robust, scalable dosage forms. Every stage is focused on achieving reproducibility, manufacturability and reliable performance throughout the product lifecycle.

With capabilities spanning conventional, complex and specialized formulations, HAB Pharma’s R&D takes products from concept through development and towards commercialization, creating a seamless pathway from scientific innovation to market-ready medicines.

R&D That Turns Science Into Solutions

Our multidisciplinary R&D framework encompasses:

Formulation Development & Technology Transfer

Development of robust formulations and seamless transfer to manufacturing.

Analytical Methods
Development

Establishment and validation of analytical methods to ensure product quality.

Compliance Quality Assurance

Ensuring adherence to quality standards across all development stages.

Intellectual Property Management

Supporting innovation through structured IP strategies.

Regulatory Affairs

Aligning development with regulatory requirements for successful approvals.

Project Management

Coordinating cross-functional activities for timely and efficient execution.

Quality Control

We also keep a detailed eye and check if there have been any neglected interactions in between the process of manufacturing to the final delivery of the goods ensuring double safety and high-quality measures.

If a cosmetic enclosure is used, tests are undertaken to check if there is any of a mixture turn adsorbed upon plastic and if any plasticizers, lubricants, pigments or stabilizers leach out of a cosmetic into a preparation.

We make sure to check and test the quality of the adhesives for an enclosure tag as a part of our quality parameters.

Our Process

From Concept to Commercialization

Literature search and pre-formulation studies

Excipient compatibility studies

Formulation development

Optimization studies

Analytical method validation

Stability studies

Technology transfer to manufacturing

Commercialization of the product

Formulation & Dosage Expertise

Our R&D capabilities span a wide range of dosage forms, enabling us to address diverse therapeutic and delivery requirements across product categories.

Dosage Form Capabilities

Solid Oral Dosage Forms: Tablets, capsules, pellets
Liquid Dosage Forms: Solutions and suspensions
Semi-Solid Dosage Forms: Creams, gels, ointments and emulsions
Injectable Dosage Forms: Solution injections, lyophilized injections, dry powder injections
Ophthalmic Dosage Forms: Eye drops and eye suspensions

Advanced & Complex
Formulation Expertise

In addition to conventional dosage forms, we possess capabilities in the development of complex and specialized formulations, supporting differentiated and high-value product development. This combination of broad formulation capabilities and advanced expertise enables the development of robust, scalable, and commercially viable pharmaceutical products.

Our expertise includes:

Quality by Design (QbD) Driven R&D Process

Every stage of the pipeline above is guided by Quality by Design (QbD) principles. Rather than testing quality into a product after the fact, we build it in from the start combining active ingredients with suitable excipients through structured lab-scale trials, so that each formulation is optimized, reproducible, and ready for manufacturing before it ever leaves R&D.
This approach ensures consistency, process control, and a smooth transition from prototype to commercial-scale production.

Quality Built Into Every Stage

At HAB Pharma, quality is embedded across the entire R&D lifecycle. From early-stage development and analytical evaluation to documentation and technology transfer, we follow defined protocols, maintain data integrity, and conduct structured technical reviews to ensure consistency, reliability, and compliance.
Our quality framework incorporates stage-wise technical and peer reviews, analytical method validation, comprehensive documentation, and routine equipment calibration and validation.
These measures enable the early identification and resolution of potential deviations, strengthening the robustness of our products before technology transfer to manufacturing. By integrating quality into development from the outset, HAB Pharma ensures that every product is built on a foundation of scientific rigor, process discipline, and readiness for scale-up and commercialization.

Targeted Therapies. Measurable Outcomes. Global Health.

Addressing critical therapeutic areas by combining precision research, advanced biotechnology, and patient-centric healthcare solutions worldwide.

Protecting Innovation & Intellectual Property

Intellectual property management is an integral part of our product development framework. We follow a structured approach to identifying, evaluating, protecting, and monitoring intellectual property throughout the development lifecycle, with a focus on safeguarding formulation know-how, process innovation, and other proprietary assets.

IP Monitoring & Governance

Intellectual property assets and relevant third-party developments are monitored as part of our broader IP governance framework. Where appropriate, suitable measures are undertaken to protect the Company's intellectual property rights and proprietary information against unauthorized use or potential infringement.

Through this structured approach, intellectual property considerations are incorporated into product development while protecting proprietary knowledge and supporting sustainable innovation.

R&D That Turns Science Into Solutions

Our multidisciplinary R&D framework encompasses: