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Tailored Fill & Finish process. Fill & Finish

Through our fill and finish facility we will be able to offer you customized and patient-centric filling of small-scale peptide drug product (i.e. therapeutics). Our primary focus is ensuring regulatory compliance, adhering to all relevant standards, including current Good Manufacturing Practices (cGMP). This commitment guarantees the highest levels of peptide therapeutic quality and safety.

In the future we will be able to provide individualized, GMP-grade, peptide vaccine products for clinical trials.

Receive notice when our Fill & Finish facility opens
Coming in 2024

Our commitment Peptide-based, medicinal products for clinical use

Feel free to contact our business development today to experience the difference that expertise, compliance, and customer-centricity can make in your fill and finish process.

Together, let's bring your peptide therapeutic into clinical trial.

 

Technology

We take pride in building our state-of-the-art infrastructure, cutting-edge equipment, and advanced technologies, tailored to meet your specific clinical trial requirements. Our continual investment in capabilities will enable us to deliver excellence.

Quality Control

Quality control is at the heart of what we do. Our meticulous approach encompasses comprehensive quality control procedures, such as process validation, batch testing, and robust quality assurance programs. Our application for the ISO 9001 certification exemplifies our unwavering commitment to delivering the highest quality standards.

Customization

Understanding that every peptide therapeutic is unique, we offer a range of customization options, including different packaging formats and labeling solutions, all tailored to your specific requirements.

Customer Focus

Collaboration and communication are paramount. We value your partnership and go above and beyond to foster transparency, responsiveness, and a genuine understanding of your unique needs.

Good Manufacturing Practice (GMP)

Highly qualified and trained personnel

Our manufacturing process will be executed by personnel who possess extensive qualifications and training.

Adequate premises and spaces

Our manufacturing facility will be thoughtfully designed with sufficient space to facilitate the hygienic and efficient production of medicinal products. We prioritize an environment that fosters productivity and adheres strictly to rigorous quality standards.

Appropriate equipment and services

We will utilize state-of-the-art equipment, specially selected for the GMP production of peptides. Our equipment will undergo regular maintenance to maintain consistent peptide therapeutic quality.

Correct materials, containers, and labels

We will meticulously choose top-quality materials, containers, and labels for our manufacturing process. Our innovative labeling and handling system will safeguard the integrity of your peptide therapeutics.

Approved procedures and instructions, aligned with the Pharmaceutical Quality System

Our manufacturing process will abide strictly by approved procedures and instructions. Our unwavering dedication to compliance and quality control will ensure that your peptide therapeutics consistently meet the highest quality standards.

Suitable storage and transportation

We will prioritize proper storage and transportation conditions to preserve the quality of your peptide therapeutics from our facility to your clinical trial site.

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Intavis Peptide Services

Peptides tailored to your research Order your peptides

Click order and a form will pop-up so you can enter your sequence directly. Alternatively upload a document listing your peptides or conjugates.