Ointment Manufacturing

Advanced CDMO solutions for semi-solid pharmaceutical formulations. End-to-end third party pharmaceutical manufacturing with automated precision systems.

Comprehensive Ointment Manufacturing Solutions

Ointment manufacturing requires controlled processing, uniform mixing, and validated filling systems to ensure product consistency and stability. As a specialized CDMO partner, Delwis operates an advanced automatic ointment manufacturing plant designed for precision and scalability. Our infrastructure supports pharmaceutical companies seeking a reliable ointment manufacturing plant manufacturer with strong regulatory compliance.

We deliver compliant third party pharmaceutical manufacturing solutions tailored for semi-solid formulations across domestic and international markets.

Our Vision

Quality

Ointment manufacturing demands strict environmental controls, validated homogenization, and consistent viscosity management. Our WHO-GMP aligned automatic ointment manufacturing plant ensures uniform blending, controlled heating, and accurate tube filling under monitored conditions. Every batch undergoes comprehensive in-process testing and finished product quality evaluation before release.

  • WHO-GMP compliant ointment manufacturing facilities
  • Automatic ointment manufacturing plant with validated systems
  • In-house analytical and microbiological testing laboratories
  • Controlled environment mixing and homogenization processes
  • Comprehensive batch documentation and traceability protocols

Our Approach

We combine technical expertise in semi-solid formulations with commercial scalability to deliver reliable CDMO partnerships. Our third party pharmaceutical manufacturing model ensures seamless technology transfer, validated scale-up, and predictable supply performance.

Flexible batch manufacturing for domestic and export markets
Process optimization for efficient semi-solid production
Integrated production planning for uninterrupted supply continuity

Augmented Services Along With Quality Medicines

Beyond ointment manufacturing, we provide regulatory and operational support that strengthens market readiness. Our third party pharmaceutical manufacturing framework ensures quality, compliance, and commercial reliability.

Regulatory Dossier Support

Comprehensive documentation aligned with domestic and international regulatory standards.

Technology Transfer Management

Structured onboarding for compliant semi-solid formulation transfer.

Stability Programs

Accelerated and real-time studies ensuring shelf-life validation.

Tube Filling & Packaging

Precision tube filling with tamper-evident, export-ready packaging.

Why Delwis

Delwis stands as a trusted ointment manufacturing plant manufacturer delivering compliant and scalable CDMO solutions. Our automated systems, regulatory alignment, and commercial discipline support confident outsourcing decisions.

Specialized expertise in ointment manufacturing
Advanced automatic ointment manufacturing plant infrastructure
WHO-GMP compliant production and validation systems
Strong regulatory documentation and audit preparedness
Scalable capacity for high-volume semi-solid production
Reliable timeliness and long-term CDMO partnerships

Whom We Work With

We collaborate with pharmaceutical organizations seeking compliant and scalable CDMO partnerships for ointment manufacturing. Our infrastructure supports both emerging and established brands.

Our Ideal Partners

Pharmaceutical companies expanding semi-solid product portfolios

Global firms seeking third party pharmaceutical manufacturing partnerships

Organizations requiring compliant CDMO scale-up solutions

Export-focused companies targeting regulated markets

Product NameCompositionClass
Clobotic OintmentClobetasol 0.05% + Salicylic acid 3.0% Cream

Ointments

Start Your Ointment Manufacturing Project

If you are looking for a reliable ointment manufacturing plant manufacturer or automatic ointment manufacturing plant partner for third party pharmaceutical manufacturing, Delwis Healthcare is ready to support your requirements.

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FAQs

Below are common questions from pharmaceutical companies evaluating our CDMO and third party pharmaceutical manufacturing capabilities for ointments.

Yes, our ointment manufacturing facilities operate under WHO-GMP guidelines with validated mixing, homogenization, and filling systems supported by comprehensive quality documentation.