Skip to Content


Services

API Procurement & Supply Chain 

We support pharmaceutical companies in identifying and sourcing high-quality Active Pharmaceutical Ingredients from globally compliant manufacturers. Our network includes qualified API suppliers with regulatory approvals from major health authorities.

  • Supplier Identification
  • Vendor Qualification Support
  • Regulatory Documentation
  • Supply Chain Management

Generic/Novel Product Development 

Our scientific team provides comprehensive support in developing generic/novel and all types of pharmaceutical formulations, including formulation design, analytical development, stability studies, and scale-up for commercial manufacturing. 

  • API, Excipient & Packaging Selection
  • Formulation Development
  • Analytical Method Development
  • Stability Studies

Technology Transfer & Site Transfer

Our team supports seamless transfer of pharmaceutical products and manufacturing processes between development laboratories and commercial manufacturing facilities approved by global regulatory agencies.

  • WHO-GMP, EU-GMP, US-FDA, UK-MHRA Facility
  • Analytical Method Transfer
  • Manufacturing Process Transfer
  • Validation Support

Contract Manufacturing (CMO) 

We collaborate with globally recognized cGMP manufacturing facilities to support production of all types of pharmaceutical, nutraceutical, cosmeceutical, and veterinary products.

  • Manufacturing Capabilities / Dosage Forms
  • Solid, Liquid, Injectable, Others
  • Nutraceutical & Wellness Products
  • Veterinary

CRO & Clinical Research Services 

Our clinical research support includes end-to-end management & coordination of bioequivalence and bioavailability studies required for regulatory approval of generic products.

  • CRO Selection
  • BA/BE Study Design & Coordination
  • Study Monitoring
  • Data Management and Reporting

Regulatory & Dossier Services 

We provide regulatory support including CTD dossier preparation, regulatory strategy development, and product registration support in multiple international markets.

  • Dossier Preparation
  • Regulatory Strategy
  • Product Registration Support
  • Licensing & Business Development

CORE AREA


Pharmaceutical 


Generic product development and manufacturing support for global regulated / semi-regulated markets. 

We optimize the end-to-end value chain for generic small and large molecule therapeutics including the high-end specialized products segments. 

Our core services encompass the strategic procurement of niche Active Pharmaceutical Ingredients (APIs), advanced Formulation Development (F&D), Dossier design, Technology Transfers (TT), and the management of Abbreviated New Drug Applications (ANDAs). 

We bridge the transition between laboratory validation and scalable commercial manufacturing.

Securing global market approval for generic products requires definitive proof of therapeutic equivalence. 

PharpleQ coordinates complete Clinical Studies workflows and Bioequivalence (BE) studies through fully accredited Contract Research Organizations (CROs).

We propose the suitable Clinical Study Design, Protocols, Bioanalytical Method Development / Validation, and Pharmacokinetic evaluations through Complete Study Monitoring to deliver impartial, regulatory-ready current Good Clinical Practice (cGCP) audit reports that satisfy global health authorities.

  • Full CTD/eCTD/ACTD Dossiers
  • Complex Generic Formulations
  • Rx to OTC Switch Strategies
  • Sterile & Oncology Supply


Nutraceutical 


Development and commercialization of nutritional supplements and functional health products. 

Responding to the global demand for preventative health solutions, we source and develop premium-grade, highly bio-available dietary elements, botanical extracts, herbal medicines and functional food ingredients. 

Our formulations prioritize molecular stability, precise ingredient standardization, and strict alignment with international food safety and labelling parameters.

  • Vitamin & Mineral Blends
  • Nutritional Supplements
  • Functional Food Ingredients
  • Herbal & Botanical Extracts


Cosmeceutical


Dermatological, wellness and cosmetic formulations developed with pharma grade quality standards. 

We serve the intersections of dermatology and topical care by providing scientifically backed, high-purity active skin elements.

Our services support brands in engineering high-performance topical formulations, ensuring rigorous studies, skin-permeation optimization, and prolonged shelf-life stability indexes.

  • Advanced Derma-Formulations
  • Anti-Aging & SPF Efficacy
  • Scalp, Hair, Skin-Care Tech
  • Regulatory Safety Dossiers



Veterinary 


Development and manufacturing support for veterinary medicines and animal health products.

PharpleQ extends its specialized procurement and regulatory infrastructure to the animal health sector. 

We manage the sourcing of bulk veterinary APIs, feed additives, and specialized therapeutic agents, ensuring strict adherence to separate veterinary regulatory frameworks, maximum residue limits (MRLs), and safety compliance patterns.

  • Antibiotics & Nutrients
  • Companion Animal Health
  • Feed Additives & Premixes
  • WHO and other GMP Veterinary Plants