Formulation & Development Services

OUR FORMULATION & DEVELOPMENT CAPABILITIES

Comprehensive Formulation & Development Solutions

  • Controlled release and sustained release formulations
  • Excipient compatibility selection and optimization
  • Formulation development for new chemical entities (NCE) using QbD approaches
  • Lab scale, pilot plant, and scale-up production
  • Novel drug delivery systems (NDDS) for existing drugs
  • Optimization of existing formulations
  • Technology transfer and commercial production support
  • Formulation and development of solid orals, liquids, transdermals, water-soluble films, gummies, topical products, parenterals, NDDS, and cosmetics

We develop a wide range including solid orals, liquids, transdermals, parenterals, NDDS, and cosmetic formulations.

Yes, we use Quality by Design (QbD) approaches to ensure robust and optimized formulations.

Yes, we support lab-scale development, pilot batches, scale-up, and technology transfer for commercial manufacturing.

Yes, we develop NDDS solutions to enhance drug performance and delivery.

Yes, we provide formulation optimization services to improve stability, performance, and compliance.

ADVANCED FORMULATION & DEVELOPMENT

Smart Formulations. Confident Outcomes.

Formulation and development play a critical role in transforming active compounds into safe, effective, and market-ready products. At Accuprec, we provide end-to-end formulation and development services designed to support new product development, optimization, and commercialization.

Our expertise includes controlled and sustained release formulations, excipient compatibility studies, and formulation development for new chemical entities (NCEs) using Quality by Design (QbD) approaches. We also support scale-up, pilot production, and technology transfer to ensure smooth transition from laboratory to commercial manufacturing.

From novel drug delivery systems to optimization of existing formulations, our services are tailored to deliver performance, stability, and regulatory compliance across a wide range of dosage forms.

Our Process

Our Approach to Accurate & Compliant Testing

01

Requirement Understanding

We begin by understanding your product, testing requirements, and regulatory objectives to define a clear analytical strategy.

02

Method Development & Planning

Our team develops and optimizes analytical methods, ensuring alignment with ICH, USP, and global regulatory standards.

03

Testing & Analysis

Samples are tested using advanced instrumentation such as LC-MS/MS, ICP-MS, and other validated techniques for accurate results.

04

Reporting & Compliance Support

We deliver detailed, audit-ready reports and provide support for regulatory submissions and compliance requirements.

Why us?

You’ll Know What

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