Clearis Soap is a specialized topical formulation designed for pharmaceutical applications, incorporating 1.0% w/w permethrin as the active ingredient. The formulation is based on a stable, water-soluble soap matrix that ensures uniform dispersion of the active component. Permethrin, a synthetic pyrethroid, is known for its broad-spectrum insecticidal and acaricidal properties, making it a preferred choice for pharmaceutical-grade products requiring efficacy against parasitic infestations. The soap base is formulated with surfactants, emulsifiers, and preservatives to enhance cleansing properties while maintaining the stability and potency of permethrin. The formulation process involves precise blending, homogenization, and quality control checks to ensure consistency, purity, and compliance with pharmaceutical standards. The product’s pH-neutral formulation ensures compatibility with skin and environmental conditions, while its non-greasy texture facilitates easy application and rinsing.
Manufacturing Capability
Our manufacturing infrastructure is designed to meet the stringent requirements of pharmaceutical production, with a focus on precision, scalability, and compliance. The facility is equipped with state-of-the-art equipment, including high-speed mixers, homogenizers, and temperature-controlled storage systems, ensuring consistent product quality. Sterile processing capabilities are maintained through ISO-certified cleanrooms and validated aseptic techniques, ensuring contamination-free production. All manufacturing processes adhere to Good Manufacturing Practice (GMP) guidelines, with rigorous validation protocols for equipment, processes, and raw materials. The facility supports scalable production, enabling seamless transitions from small-batch trials to large-scale bulk manufacturing. Quality systems are integrated throughout the production lifecycle, with real-time monitoring and documentation to ensure traceability and regulatory compliance.
Available Strengths and Packaging
Composition: Permethrin 1.0% w/w
Packaging: 75gm
Clearis Soap is available in a single strength of 1.0% w/w permethrin, tailored for pharmaceutical applications requiring precise dosing. The 75gm packaging is designed for efficient distribution and storage, ensuring product integrity during transit and shelf life.
Contract Manufacturing / Third Party Manufacturing
As a trusted manufacturer, we offer comprehensive contract manufacturing, private label production, and third-party manufacturing services to meet the diverse needs of pharmaceutical buyers. Our facility is equipped to handle custom formulations, including variations in active ingredient concentrations, excipient compositions, and packaging specifications. We support private label manufacturing, enabling clients to brand products under their own trademarks while leveraging our expertise in pharmaceutical formulation. Third-party manufacturing services include full-scale production, quality assurance, and regulatory documentation, ensuring compliance with global standards. Our flexible production model allows for rapid prototyping and scalability, making us an ideal partner for pharmaceutical companies seeking to expand their product portfolios.
Quality Assurance
Our quality assurance framework is built on rigorous testing, analytical validation, and adherence to pharmaceutical standards. Every batch of Clearis Soap undergoes comprehensive quality control checks, including physical, chemical, and microbiological testing. Analytical validation is performed using advanced techniques such as high-performance liquid chromatography (HPLC) to confirm the purity and potency of permethrin. Microbial testing ensures the absence of contaminants, while stability studies validate shelf life under varying conditions. All quality control processes are documented and traceable, ensuring compliance with pharmacopeial standards such as USP, EP, and BP. Our commitment to quality is further reinforced by regular internal audits and third-party inspections, ensuring consistent product excellence.
Regulatory Compliance
We ensure full compliance with global regulatory frameworks, including Good Manufacturing Practice (GMP), World Health Organization (WHO) guidelines, and international standards such as ISO 9001 and ISO 14001. Our manufacturing processes adhere to GMP requirements, with validated procedures for raw material sourcing, production, and packaging. Compliance with WHO guidelines ensures that our products meet the standards for quality, safety, and efficacy in international markets. Additionally, our facility is certified under ISO 9001 for quality management and ISO 14001 for environmental management, reflecting our commitment to sustainable and responsible manufacturing. These certifications enable seamless export to regulated markets and facilitate compliance with regional and national regulatory bodies.
Global Supply Capability
Our global supply capability is supported by a robust international distribution network, bulk supply capacity, and reliable supply chain infrastructure. We specialize in exporting pharmaceutical products to over 50 countries, with logistics partnerships ensuring timely delivery to remote and urban markets. Bulk supply capacity is optimized through automated packaging systems and efficient inventory management, enabling large-scale orders without compromising quality. Our supply chain reliability is further enhanced by real-time tracking systems, contingency planning, and compliance with international shipping regulations. This ensures uninterrupted supply to pharmaceutical distributors, exporters, and contract manufacturers, even in demanding global markets.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturing partners choose us for our expertise in high-quality, compliant manufacturing, scalable production, and global supply solutions. Our facility’s adherence to GMP, WHO, and ISO standards ensures that products meet the rigorous requirements of international markets. We offer end-to-end services, from formulation development to global distribution, reducing the complexity of supply chain management for our clients. Our commitment to innovation, sustainability, and customer-centric solutions positions us as a reliable partner for businesses seeking to expand their pharmaceutical portfolios.
Bulk Supply Inquiry
We provide bulk supply capabilities for Clearis Soap, tailored to meet the needs of pharmaceutical buyers. For inquiries regarding large-scale orders, please contact our team at info@delwishealthcare.com.
FAQs
What manufacturing standards does Clearis Soap comply with?
Clearis Soap is manufactured in accordance with GMP, WHO guidelines, and ISO 9001/14001 standards, ensuring compliance with global pharmaceutical regulations.
Can Clearis Soap be customized for different packaging sizes?
Yes, we offer flexible packaging options, including the standard 75gm size, and can accommodate custom packaging requirements based on client specifications.
What quality control measures are in place for Clearis Soap?
Each batch undergoes rigorous testing, including HPLC analysis, microbial testing, and stability studies, to ensure compliance with pharmacopeial standards.
Is Clearis Soap suitable for export to international markets?
Yes, our compliance with WHO, GMP, and ISO standards ensures that Clearis Soap meets the regulatory requirements for export to global markets.
Can you provide third-party manufacturing services for Clearis Soap?
Yes, we offer contract manufacturing and private label production services, enabling clients to brand and distribute the product under their own trademarks.
What is the shelf life of Clearis Soap?
The shelf life of Clearis Soap is validated through stability studies, ensuring product efficacy and safety for the recommended storage period.
Do you offer bulk supply options for Clearis Soap?
Yes, we provide bulk supply capabilities to meet the needs of pharmaceutical buyers, with scalable production to accommodate large orders.
How do you ensure supply chain reliability for international shipments?
Our logistics partnerships and real-time tracking systems ensure timely and reliable delivery, with contingency plans to address supply chain disruptions.
Can Clearis Soap be formulated with different active ingredient concentrations?
While Clearis Soap is standardized at 1.0% w/w permethrin, we can develop custom formulations upon request, subject to regulatory approval.
What certifications do you hold for pharmaceutical manufacturing?
We are certified under GMP, WHO, ISO 9001, and ISO 14001, reflecting our commitment to quality, safety, and environmental responsibility.
