Our Services
Contract Manufacturing
As the industry's market partner in manufacturing, we offer seamless end-to-end services that are fully accustomed to our client's needs.
Product Licensing
Interphil-developed formulations are available for out-licensing opportunities with customers searching for products to market under their brands or house brands.
Product & Process Development
Our pursuit for scientific and technical excellence, achieved through our highly competent teams and application of our various manufacturing capabilities, has led to the successful development and introduction of new products and line extensions for our partners.
Quality Management
Interphil's Quality Management system maintains its robustness by following essential key elements such as Quality Policy, Quality Risk Management and Quality Objectives also taking into account all available guidelines and regulations in the Pharmaceutical Industry. This facilitates Interphil's innovation along with continual improvement thereby ensuring high product quality and minimizing risk of product recall.
Regulatory Affairs
We ensure that the company and its clients adhere to appropriate licensing, marketing and legal compliance standards.
Commercial Solutions
As part of Interphil's commitment to become your strategic partner, we also offer sales and marketing services to ensure successful brand commercialization.
- Our Services
- Contract Manufacturing
- Product Licensing
- Product and Process Development
- Quality Management
- Regulatory Affairs & Advisory
- Commercial Solutions
Our core capabilities

Sourcing & Procurement

Quality Management

Manufacturing & Packaging
Your market partner in pharmaceutical manufacturing

Technology & Site Transfer

Warehousing & Logistics

SOURCING, PLANNING & PROCUREMENT, SUPPLIER MANAGEMENT
We manage over 500 suppliers in our global network ensuring the quality of materials and supply continuity.

MANUFACTURING & PACKAGING
Our fully-equipped production facilities allow conversion to multiple forms and various packaging presentations

Dry Products
- Tablets (plain, sugar-coated, film-coated, chewables)
- Capsules (hard gel and soft gel)
- Lozenges
- Powder and Granules
Liquids
- Orals (Syrups, Suspensions, Solutions, Elixirs)
- Topical (Mouthwash, Gargle, Solution)
- Suspensions


Semi Solids and Topicals
- Creams and Ointments, Gels and Pastes
- Personal Care (Shampoo, Lotion, Wash)
- Cosmetics
- Suppositories and Pessaries
Beta Lactams
- Dedicated manufacturing plant for Cephalosporin production
- Capsules
- Tablets (Film-Coated)
- Powder for Suspension


SoftGels
- Capsules in bulk or in blister/strip packaging
QUALITY ASSURANCE
Our stringent quality system ensures that all products are produced to the highest quality standards.

WAREHOUSING, EXPORT & LOGISTICS
We make sure that the quality of products is maintained until the end of the supply chain through our trusted logistics partners.
We are committed to following the standards set by PIC/S GMP to achieve the highest level of quality and regulatory compliance.

Product Licensing
We offer a range of high quality pharmaceuticals (prescription, over-the-counter, home remedies), food supplements and personal care products in a variety of dosage forms, formats and packaging presentations.
Our highly qualified team assists customers by providing technical support with product registration and other testing, quality and regulatory requirements.

Provide Turnkey Solutions
We provide turnkey solutions for many formulation and manufacturing needs and challenges to help our clients meet their business requirements.


Analytical Method Development
Our laboratories ensure that products undergo rigorous trials, process validation, analytical method development and validation, stability testing and independent or collaborative product interchangeability testing aligned with local and international regulatory guidelines and quality standards.
Full Quality System Services
- Material Quality Control - Testing of raw imported bulk and packaging components, in-process, semi-finished and finished products.
- Documentation - Preparation of Technical Dossiers, Master Batch Documentation, Manufacturing/ processing instructions and Packaging orders, Validation documents, Test Methods and Specification sheets.


- Validation - Process and Non Process Validation (equipment, facility, and utility systems including cleaning validation), Method Validation, Method Development and Verification, Computerized System Validation
- Product Release - Batch record review to appropriately determine satisfactory conformity to its finished products specification prior release.
- Product Evaluation - Stability testing, Annual Product Review, Pharmacovigilance and Handling of Product Complaint
This is achieved by:
- Keeping up to date with all legal and regulatory policies, procedures and guidances.
- Maintaining and understanding all scientific and technical requirements of all healthcare products.
- Obtaining and maintaining necessary licenses and marketing authorizations.
- Advising on legal and scientific restraints or challenges and requirements.
- Participating in the development and approval of product marketing concepts and packaging prior commercialization.

Strategizing Success
Guided by the brand owner's strategic direction, we can create successful ethical promotion strategies, trade and consumer programs, and digital marketing solutions.
