Our Services
Comprehensive pharmaceutical solutions tailored to meet your needs
Contract Manufacturing Excellence
Holiness Pharmaceutical is a trusted Pharmaceutical Contract Manufacturing Company committed to delivering WHO–GMP certified quality across all our formulations.
With a legacy of quality, reliability, and innovation, Holiness Pharmaceutical has emerged as a preferred partner for leading healthcare and pharmaceutical organizations across both domestic and international markets.
Backed by a team of highly qualified and experienced professionals, we offer customized formulation solutions tailored to meet our clients' specific requirements — from concept to commercial production.
Our Manufacturing Strengths
State-of-the-art facilities built in compliance with WHO–GMP standards
Fully computerized systems for precision-controlled manufacturing
Capability to produce sterile and general dosage forms, covering all therapeutic segments
Specialized and dedicated production lines for Beta-Lactam and Cephalosporin formulations
Expert technical teams in Quality Control, Quality Assurance, and Product Development
Proven track record of on-time delivery, regulatory compliance, and consistent quality
As a focused contract manufacturing company, Holiness Pharmaceutical has earned the trust of its clients by offering high-quality, cost-effective, and scalable production solutions — making us a preferred partner for long-term growth and collaboration.
Production Capacity
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Yearly Capacity
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Yearly Capacity
Holiness Pharmaceutical continues to set benchmarks in pharmaceutical contract manufacturing through its uncompromising quality standards, cutting-edge infrastructure, and commitment to excellence.
Third Party Manufacturing
At Holiness Pharmaceutical, we specialize in providing WHO–GMP compliant pharmaceutical products through Third Party Manufacturing Services in India for our domestic and international clients.
With our large-scale production capacity, modern infrastructure, and highly qualified team of professionals, we are fully equipped to meet diverse third party manufacturing requirements — efficiently, cost-effectively, and with uncompromising quality.
We ensure strict quality control at every stage of production — from procurement of raw materials to formulation development, testing, and export — ensuring that each product meets global regulatory standards.
Our 3rd Party Manufacturing Process
Formulation Approval
Obtain product approval from the Drug Department
Procurement of Raw Materials
Source high-grade raw materials from approved vendors
Formulation & Production
Manufacture under WHO–GMP certified conditions with modern equipment
Testing & Export
Conduct thorough quality checks and prepare products for export
Commitment to Quality & Partnership
At Holiness Pharmaceutical, our focus is on building long-term partnerships by offering quality branded medicines and generic formulations tailored to global healthcare needs.
Through our collaborative approach, regulatory excellence, and customer-first philosophy, we have become a trusted third-party manufacturing partner for several leading pharmaceutical companies worldwide.
Regulatory Services
Expanding into international pharmaceutical markets requires deep expertise and a clear understanding of complex global regulatory frameworks. At Holiness Pharmaceutical, our Drug Regulatory Affairs (DRA) team provides end-to-end support to help clients navigate these challenges seamlessly.
Our regulatory experts assist companies in planning, managing, and executing pharmaceutical and medical product development programs in full compliance with country-specific regulatory requirements.
By developing strategic regulatory pathways from the early stages of product development, we help ensure swift approvals, smoother registrations, and faster product launches across multiple markets.
Our Regulatory Service Portfolio
Registration Services
- Preparation, review, and submission of Drug Master Files (DMFs) in CTD format
- Dossier writing, review, and registration in accordance with international guidelines
- Support for COA, COPP, Notarization, and other legal documentation
- Coordination with regulatory authorities to streamline the approval process
Post-Approval Services
- Product re-registration and site renewals as per regulatory schedules
- Post-approval lifecycle management to ensure ongoing compliance
- Change management, report compilation, and publishing support
Pre-Registration Services
- Drug Product DMF development and documentation
- Preparation and submission of technical and regulatory documents
- Content creation, data verification, and dossier compilation for targeted markets
With a strong foundation in global compliance and documentation excellence, Holiness Pharmaceutical ensures that every product meets international regulatory standards — enabling our clients to enter and sustain a successful global presence with confidence.
Our goal is to simplify the regulatory journey so you can focus on what truly matters — bringing quality medicines to the world.