gel Manufacturing

End-to-end third party pharmaceutical manufacturing for aloe vera gel, neutrogena hydro boost gel cream equivalents, and advanced hydrating gel portfolios. Built for regulatory compliance, scalable production, and commercial reliability.

Comprehensive Gel Manufacturing

Topical gels including aloe vera gel, neutrogena hydro boost gel cream type formulations, and specialized hydrating gel products require advanced formulation expertise and controlled manufacturing environments. As a CDMO partner, Delwis delivers third party pharmaceutical manufacturing solutions for dermatological and cosmetic-grade gel formulations.

Our facilities support consistent viscosity control, formulation stability, and scalable commercial manufacturing of complex gel products.

Our Vision

Quality

Manufacturing aloe vera gel, neutrogena hydro boost gel cream equivalents, and hydrating gel products demands strict process validation and microbial control. Our production infrastructure operates under WHO-GMP guidelines to ensure formulation stability, consistency, and product safety. Each manufacturing batch undergoes rigorous in-process monitoring and finished product quality verification.

  • WHO-GMP compliant manufacturing units
  • Validated gel mixing, homogenization, and filling systems
  • Advanced microbiological and stability testing laboratories
  • Controlled environmental and contamination prevention protocols
  • Complete batch traceability and documentation systems

Our Approach

We combine formulation science, scale-up expertise, and commercial manufacturing insight to deliver dependable CDMO solutions for gel formulations. Our model supports seamless technology transfer, optimized production batches, and predictable supply continuity.

Flexible batch manufacturing for domestic and international hydrating gel markets
Process optimization to ensure viscosity stability and cost efficiency
Integrated supply chain management supporting uninterrupted commercial distribution

Augmented Services Along With Quality Medicines

Beyond manufacturing, we deliver strategic services that strengthen commercial success and product lifecycle management.

Regulatory Dossier Support

Comprehensive documentation aligned with global gel formulation regulatory requirements.

Technology Transfer Management

Structured onboarding ensuring compliant and efficient product transitions.

Stability Studies

Accelerated and real-time programs ensuring long-term gel formulation stability.

Packaging & Serialization

Export-ready packaging systems with full traceability and tamper-evident protection.

Why Delwis

Delwis is a trusted CDMO partner for gel formulation manufacturing, supporting pharmaceutical companies with scalable infrastructure and regulatory excellence. Our operational discipline ensures consistent product quality, supply continuity, and long-term manufacturing partnerships.

Specialized expertise in aloe vera gel and hydrating gel manufacturing
WHO-GMP aligned production and quality systems
Extensive third party pharmaceutical manufacturing experience
Strong regulatory documentation and audit preparedness
Scalable infrastructure for high-volume gel production
Reliable supply timeliness supporting global product launches

Whom We Work With

We collaborate with pharmaceutical companies seeking compliant and scalable CDMO partnerships for aloe vera gel, hydrating gel, and advanced topical gel products.

Our Ideal Partners

Branded pharmaceutical companies expanding dermatology and hydration portfolios

Global firms seeking third party pharmaceutical manufacturing for gel formulations

Organizations requiring regulatory-compliant CDMO scale-up capabilities

Export-focused pharmaceutical marketing companies launching gel products

Product NameCompositionClass
Ashru GelCarboxy Methyle Cellulose 1% W/V+ Glycerine Eye drops.

Ophthalmology, Gels

Start Your Gel Manufacturing Project

Partner with Delwis for reliable third party pharmaceutical manufacturing of aloe vera gel, hydrating gel, and neutrogena hydro boost gel cream equivalent formulations.

No form fields available.

FAQs

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

Yes, our manufacturing facilities operate under WHO-GMP guidelines with validated gel processing equipment, controlled manufacturing environments, and documented quality assurance protocols.