After the Winter Break, We’re Moving Full Speed Ahead as CDMO
January 17, 2025
Winter may have surrounded us in darkness, but here at Zelmic, we’re seeing the light – in the form of new opportunities and exciting projects for 2025! After a well-deserved winter break, we’re back, energized, and ready to continue driving innovation and excellence in topical product development, analytical chemistry, in vitro models, and IMP manufacturing in our GMP unit.
Our Offering – Expertise and Flexibility Tailored to Your Needs
🔬 Topical Product Development
We provide end-to-end solutions to create innovative dermatological and transdermal products. Our services include:
- Formulation Development: Crafting stable creams, ointments, gels, and solutions.
- Process Development: Optimizing manufacturing processes for scalability and reproducibility.
- Patent Protection: Strategically developing unique formulations to secure patents.
🧪 Analytical Chemistry
Our analytical team utilizes cutting-edge technologies and methodologies to ensure the highest quality at every stage of product development:
- Quality Control (QC): Rigorous testing to guarantee product safety and efficacy.
- Stability Studies: Assessing product durability and performance under various conditions.
- Regulatory Analysis: Comprehensive data and documentation compliant with EMA and FDA requirements.
💻 In Vitro Models for Skin and Drug Testing
We specialize in in vitro methods that provide critical insights into your product’s performance before clinical trials. Our offerings include:
- Skin Permeation Testing: Measuring the penetration of active ingredients through the skin.
- IVPT and IVRT: (In Vitro Permeation Testing and Release Testing) validated methods for evaluating release and absorption.
- Customized Models: Tailored testing solutions for unique formulations.
🏭 IMP Manufacturing in Our GMP Unit
Our state-of-the-art Class D GMP facility is designed to meet the highest standards for manufacturing clinical trial materials:
- Non-sterile Topical Product Manufacturing: Including creams, ointments, gels, and solutions.
- Batch Documentation and Traceability: Full compliance with GMP standards.
- Fast Turnaround Times: Efficient processes to reduce time-to-clinic.
Why Choose Zelmic?
As a specialized CDMO, we bring over 20 years of experience in topical product development and a dedicated focus on supporting small companies and startups:
- Comprehensive Services: From concept to clinical trials and registered products.
- Flexibility and Speed: Tailored solutions with quick turnaround times.
- Scientific and Regulatory Expertise: Ensuring your product meets global standards.
Ready to Take the Next Step?
Get in touch with us today to see how Zelmic can help turn your ideas into reality and achieve success in the market.
👉 Learn more about our services at www.zelmic.se.
Wishing you a successful and inspiring year ahead,
The Zelmic Team
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