Tablets & Capsules
Immediate and extended-release formulations in standard and custom sizes.
Our Services
What We Offer
Three Core Services, One Trusted Partner
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.
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.
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
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.
Immediate and extended-release formulations in standard and custom sizes.
Oil-based and specialty active encapsulation with precision fill control.
Aqueous and non-aqueous liquid formulations with cold-chain capability.
Single-dose sachets including effervescents, nutraceutical blends, and ORS.
Semi-solid topical preparations including medicated and cosmeceutical grades.
Traditional herbal distillate preparations under DRAP-registered standards.
Service 02
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.
Vitamins, minerals, amino acids, and functional ingredients in optimal delivery formats.
Standardized plant extracts with validated active content for consistent efficacy.
Clinically studied strains in CFU-guaranteed sachets, capsules, and chewables.
ICH-guideline accelerated and real-time studies with full documentation
HPLC, UV, and microbiological testing methods developed and validated in-house.
Seamless transition from pilot batches to commercial production volumes.
Service 03
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.
Drug, nutraceutical, and herbal product registration with complete dossier management.
Support for WHO-PQ submissions for products entering international procurement.
SFDA (Saudi Arabia) and GCC MoH filings for Gulf region market entry.
End-to-end halal documentation, audit coordination, and certificate maintenance.
Variation filings, renewal management, and label update submissions.
Adverse event reporting, risk management, and signal monitoring services.
Our Process
We discuss your requirements, target markets, product category, and regulatory needs to map a clear path forward.
Our R&D team develops formulation options, runs stability studies, and confirms technical and commercial feasibility.
We prepare and submit all dossiers, manage correspondence with DRAP and international bodies, and secure approvals.
Full-scale production under GMP-certified conditions with in-process quality checks and batch release testing.
Custom labeling, primary and secondary packaging, and on-time delivery to your distribution network.
Ongoing pharmacovigilance, renewal filings, reformulation assistance, and scale-up support as your brand grows.
Certifications & Accreditations
FAQs