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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

End-to-end manufacturing solutions for pharmaceutical and nutraceutical products. Backed by modern production capabilities and strict quality controls, we deliver consistency, reliability, and precision at every stage.

Product Development

Turn your concepts into high-performance healthcare formulations. From initial development to optimization and refinement, we support innovation through research-driven expertise and rigorous testing.

Regulatory Assistance

Navigate complex regulatory requirements with clear, structured guidance. From dossier preparation to full submission compliance, we ensure your products move to market smoothly and with complete 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 handles high-volume production for a broad spectrum of pharmaceutical and nutraceutical formats. Whether you are a local brand scaling production, or an international distributor seeking a reliable manufacturing partner in Pakistan, our facility delivers consistent quality, on-time delivery, and full regulatory traceability.

Process Control

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

Certified Standard

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 build a clear, actionable roadmap.

02

Formulation & Feasibility

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

03

Regulatory Filing

We compile and submit all required dossiers, handle correspondence with DRAP, and secure approvals.

04

Manufacturing & QC

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

05

Packaging & Delivery

Custom labeling, primary and secondary packaging, and punctual dispatch straight to your distribution network.

06

Post-Launch Support

Ongoing pharmacovigilance, renewal management, reformulation support, and scale-up assistance as your brand expands.

Certifications & Accreditations

Unmatched Excellence and Expertise

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FAQs

Discover more about our services.

We manufacture a wide range of nutraceutical products on order, including tablets, hard capsules, softgel capsules, oral liquids and syrups, sachets and powders, topical creams and ointments, and traditional Arq (herbal distillate) formulations.
MOQs vary depending on the product type, dosage form, and packaging requirements. Please share your project details through our contact page, and our team will provide specific volume guidelines.
We manage the entire lifecycle of your product. Our process begins with an initial consultation, followed by R&D formulation, feasibility testing, and stability studies. Once the formulation is finalized, our regulatory team prepares and submits the necessary documentation for official approval.
We provide comprehensive regulatory assistance for DRAP (Pakistan), WHO Pre-qualification, and GCC markets, including SFDA requirements in Saudi Arabia.
Yes, our facility is both GMP-certified and Halal-certified. We also assist clients with Halal audit coordination and ongoing certificate maintenance for their products.
Yes. We offer complete private-label and third-party manufacturing solutions, including custom primary and secondary packaging, branding, and labeling tailored to your market needs.
Timelines depend on the product category, target market, and relevant regulatory authority. Once we review your product specifications and target regions, our regulatory team will provide a realistic estimated timeline.
We enforce strict Quality Assurance (QA) and Quality Control (QC) protocols at every stage of production. This includes raw material testing, in-process quality monitoring, and final batch release testing. Our operations adhere strictly to DRAP and WHO-GMP guidelines, backed by regular internal audits, rigorous documentation control, and continuous staff training.
We offer end-to-end support for custom nutraceutical formulations. Clients can either provide their own validated ingredients or leverage our established global supplier network for premium, standardized active raw materials. Our R&D team works directly with you to refine dosage, active concentration, flavor profiles, and stability to ensure market readiness.
Yes. Before scaling up to full commercial production, we manufacture small-scale pilot batches for stability testing, sensory evaluation, and initial regulatory submission. This allows you to validate formulation performance and packaging integrity while minimizing upfront risk.
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