Pakistan’s DRAP-Approved Nutraceutical, Food Supplement & Probiotic Manufacturing Facility β€” All Under One Roof

πŸ“ Location: Plot# 32, Street S-2, Industrial Estate, Rawat, Islamabad, Pakistan | πŸ“ž Call Us: +92 3331110194 | βœ‰ Email: adeptpharma@gmail.com

Research & Development

Innovation Through Expert R&D

Our state-of-the-art R&D facility and experienced team of nutraceutical scientists and technicians develop custom formulations tailored to your specific therapeutic needs. From concept to commercial-ready product, we manage the entire development process with rigorous testing and quality assurance.

Whether you need to develop a new drug formulation, improve an existing product, or create a unique dosage form, our R&D team has the expertise and equipment to bring your nutraceutical vision to life.

R&D Services

Our R&D Capabilities

πŸ§ͺ Formulation Development

Custom nutraceutical formulations optimized for efficacy, stability, and manufacturability.

πŸ”¬ Analytical Testing

Complete analytical characterization including HPLC, dissolution, content uniformity, and stability.

πŸ“Š Bioavailability Studies

In vitro and dissolution studies to predict product performance and bioavailability.

⏱️ Stability Testing

Accelerated and long-term stability studies following ICH guidelines for shelf-life determination.

πŸ’Š Dosage Form Innovation

Development of novel dosage forms: sustained-release, fast-dissolving, orally disintegrating tablets.

🧬 Natural Product Research

Herbal extract standardization and natural product formulation development.

Development Process

From concept to commercial product

1

Requirements Assessment

Understand your therapeutic goals, target indication, and specific requirements.

2

Pre-Formulation Studies

Characterize active ingredients and excipients for optimal formulation design.

3

Formulation Development

Develop and optimize formulations through multiple iterations.

4

Testing & Analysis

Comprehensive analytical testing and quality assessment.

5

Stability Studies

Conduct stability testing to determine shelf-life and storage conditions.

6

Pilot Batch & Scale-Up

Successful transition to commercial manufacturing process.

Frequently Asked Questions

How long does formulation development take?
Timeline varies from 3-6 months for straightforward formulations to 12+ months for complex development. We'll provide a realistic timeline after initial assessment.
Can you develop formulations for novel molecules?
Yes, our team has experience with innovative dosage forms and novel delivery systems. We can handle research on compounds not yet in commercial use.
What testing is included in development?
We include analytical testing, dissolution studies, content uniformity, microbiological testing, and stability studies. Additional specialized testing can be arranged.
Do you provide documentation for regulatory submissions?
Yes, complete development reports and technical documentation suitable for DRAP and international regulatory submissions are prepared throughout development.
Can you scale up from R&D to manufacturing?
Absolutely. We manage the complete transition from lab-scale development through pilot batches to commercial manufacturing with process validation.

Bring Your Nutraceutical Innovation to Life

Partner with our R&D team to develop products that meet market demands and regulatory requirements.

Discuss Your R&D Project