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  • ✅ GMP Certified & Quality Assured

Services

Our Services

Quality, Innovation & Care in Every Service

Fidelity Pharma offers end-to-end pharmaceutical and nutraceutical services — from contract manufacturing and product formulation to global regulatory support — all under one trusted roof.

What We Offer

Title

Three Core Services, One Trusted Partner

Every service at Fidelity Pharma is designed to meet the highest standards of quality, safety, and efficacy — helping you bring better healthcare solutions to market, faster.
Contract Manufacturing

Contract Manufacturing

End-to-end manufacturing solutions for pharmaceutical and nutraceutical products. Backed by modern production capabilities and controlled quality processes. Delivering consistency, reliability, and precision at every stage.

Product Development

Product Development

Turn your product ideas into carefully developed healthcare formulations. From formulation concepts to optimization and product refinement. We support innovation with research-driven development and expertise.

Regulatory Assistance

Regulatory Assistance

Navigate regulatory requirements with structured guidance and support. From documentation and submissions to compliance-related processes. Helping ensure your products move forward with clarity and confidence.

7 +

Manufacturing Specialties

60 +

Product Formulations

15 +

Years of Experience

100 +

Regulatory Approvals

Service 01

Contract Manufacturing

Private-label & third-party manufacturing across all dosage forms

Fidelity Pharma’s GMP-certified facility is equipped to handle high-volume production across a wide range of pharmaceutical and nutraceutical formats. Whether you are a local brand scaling up or an international distributor seeking a reliable manufacturing partner in Pakistan, our facility delivers consistent quality, on-time delivery, and full regulatory traceability.

Tablets & Capsules

Immediate and extended-release formulations in standard and custom sizes.

Softgel Capsules

Oil-based and specialty active encapsulation with precision fill control.

Oral Liquids & Syrups

Aqueous and non-aqueous liquid formulations with cold-chain capability.

Sachets & Powders

Single-dose sachets including effervescents, nutraceutical blends, and ORS.

Creams & Ointments

Semi-solid topical preparations including medicated and cosmeceutical grades.

Arq Formulations

Traditional herbal distillate preparations under DRAP-registered standards.

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Service 02

Product Development

Science-backed R&D from concept through scale-up

Our R&D team combines pharmaceutical science with nature-inspired innovation to create formulations that perform. From novel nutraceutical blends and evidence-based herbal combinations to precision probiotic strains and pharma-grade active delivery systems, Fidelity Pharma’s development process is rigorous, transparent, and outcome-focused — giving your product a competitive edge at launch.

Nutraceutical Formulation

Vitamins, minerals, amino acids, and functional ingredients in optimal delivery formats.

Herbal & Botanical

Standardized plant extracts with validated active content for consistent efficacy.

Probiotic Products

Clinically studied strains in CFU-guaranteed sachets, capsules, and chewables.

Stability Testing

ICH-guideline accelerated and real-time studies with full documentation

Analytical Validation

HPLC, UV, and microbiological testing methods developed and validated in-house.

Scale-Up Support

Seamless transition from pilot batches to commercial production volumes.

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Service 03

Regulatory Assistance

Expert navigation of local and international regulatory frameworks

Regulatory hurdles are one of the biggest barriers to bringing healthcare products to market. Fidelity Pharma’s regulatory affairs specialists have deep experience with DRAP, SFDA, WHO, and GCC guidelines. We take ownership of your filing strategy, dossier preparation, and authority liaison — so your product reaches market faster, with fewer surprises and full compliance.

DRAP Registration

Drug, nutraceutical, and herbal product registration with complete dossier management.

WHO Pre-Qualification

Support for WHO-PQ submissions for products entering international procurement.

GCC Market Filing

SFDA (Saudi Arabia) and GCC MoH filings for Gulf region market entry.

Halal Certification

End-to-end halal documentation, audit coordination, and certificate maintenance.

Post-Approval Changes

Variation filings, renewal management, and label update submissions.

Pharmacovigilance

Adverse event reporting, risk management, and signal monitoring services.

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Our Process

From Concept to Market
A Seamless Journey

01

Initial Consultation

We discuss your requirements, target markets, product category, and regulatory needs to map a clear path forward.

02

Formulation & Feasibility

Our R&D team develops formulation options, runs stability studies, and confirms technical and commercial feasibility.

03

Regulatory Filing

We prepare and submit all dossiers, manage correspondence with DRAP and international bodies, and secure approvals.

04

Manufacturing & QC

Full-scale production under GMP-certified conditions with in-process quality checks and batch release testing.

05

Packaging & Delivery

Custom labeling, primary and secondary packaging, and on-time delivery to your distribution network.

06

Post-Launch Support

Ongoing pharmacovigilance, renewal filings, reformulation assistance, and scale-up support as your brand grows.

Certifications & Accreditations

Certified Excellence

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FAQs

Discover more about our brand.

We manufacture pharmaceutical and nutraceutical products for other brands. This includes tablets and capsules, softgel capsules, oral liquids and syrups, sachets and powders, creams and ointments, and Arq (traditional herbal) formulations.
The minimum order quantity depends on the product and the dosage form. Please send us your requirement through the contact page, and our team will share the details with you.
We support you from your first idea to registration. We start with a consultation, then develop and test the formulation, including stability studies. After that, our regulatory team prepares and submits the documents for approval.
We provide regulatory support for DRAP in Pakistan, WHO pre-qualification, and the GCC markets, including SFDA in Saudi Arabia.
Yes. Fidelity Pharma is GMP certified and Halal certified. We can also help our clients with Halal documentation and certificate maintenance
Yes. We do private-label and third-party manufacturing. We can also arrange custom labeling and primary and secondary packaging for your product.
The time depends on the product, the market and the regulatory authority. Our regulatory team will give you an estimate after we know your product and target market.
We use controlled processes at every stage. This includes testing of raw materials, in-process quality checks and batch release testing. Our quality system follows DRAP and WHO-GMP guidelines, with regular internal audits, strong documentation control and staff training.
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