Pharma & Personal Care
Purity Needs Proof.
Activated carbon solutions for pharmaceutical, personal care and healthcare manufacturing processes.
PharMAX™
Activated carbon solutions for pharmaceutical, personal care and healthcare manufacturing processes.
PharMAX supports pharmaceutical and personal care manufacturers with activated carbon designed for purification, decolourisation and impurity control. Grades can be selected to suit production requirements while supporting quality, consistency and process reliability.
Process Applications
Personal Care Purification
Supports purification steps used in cosmetics, skincare and personal care ingredient processing.
Medical Carbon Applications
Activated carbon grades evaluated for healthcare and pharmaceutical purification requirements.
API Manufacturing Support
Designed for impurity control and decolourisation during pharmaceutical ingredient production.
What It Handles
- Colour bodies and impurities
- Unwanted odours and residues
- Pharmaceutical process streams
- Personal care ingredients
- Quality consistency requirements
Engineered to Deliver
- High Purity Grades: Produced to support demanding pharmaceutical and personal care applications.
- Controlled Performance: Consistent adsorption characteristics across production and purification processes.
- Flexible Specifications: Available in grades selected for diverse healthcare manufacturing requirements.
- Batch-wise COA: Quality documentation provided to support traceability and process confidence.
- Reliable Supply: Manufactured with consistency to support ongoing production requirements.
Performance Metrics
Purification:
Application- specific
Quality:
Batch- controlled
Grades:
Process- selected
Products Ranges
Request a
Custom Size!
Packaging
Standard Packing Options
- • 25 kg PP bags with inner liner
- • 500 kg / 550 kg jumbo bags
- • Bulk packaging on request
Delivered worldwide
Export-ready supply with documentation support and flexible logistics through warehouses and channel partners.
Frequently Asked Questions
We are building infrastructure and documentation aligned to pharma expectations; scope depends on project requirement.
Impurity profile, extractables, filtration behaviour, and repeatable documentation—validated on your actual process.
Optional third-party validation can be arranged where required.
Yes, subject to requirement and validation.
Yes. We lock specifications post-trial and plan supply for consistent production runs.
Yes. Batch-wise COA is available.
