PRONAV Clinical Services
Your All-in-One Partner for Early Phase Clinical Supply Chain Operations
Keep your clinical development programs on track with expert, bespoke consultancy, fully GMP-compliant labeling, packaging, kitting, and blinding services, with integrated document and project management solutions. PRONAV Clinical eliminates quality or supply delays, accelerating the journey of your therapeutic to clinical trials—and the patients who need it most.
PRONAV Clinical:
Expert Supply Chain Solutions for Every Stage
Capabilities Include:
1
Collaborative Onboarding & Roadmap Creation
We start by fully understanding your project’s unique challenges and objectives. Our experts then design a bespoke strategy, including a detailed supply chain product manufacturing and testing flow diagram outlining the associated quality information generated or required at each step.
2
Project Framework and Planning
Using our proprietary PROMAP software platform and based on the product and quality information flows generated in Step 1. we create a detailed and customized plan that ensures real-time visibility of each task, accelerates workflows and data transfer, facilitates direct stakeholder communication, and keeps your supply chain compliant and efficient.
3
Real-Time Oversight with PROMAP
Weekly project reviews and real-time updates ensure you’re always informed. Gain full visibility of your project with PROMAP, which simplifies workflows, tracks tasks, and mitigates risks.
4
Seamless Execution
From transfer of your bulk drug product from the CDMO for labeling and packaging at our Depot to final batch release and distribution, we ensure that every, we ensure every stage is completed with precision and compliance. Our team identifies and resolves potential challenges before they arise, offering innovative solutions to streamline operations.
5
On-Time Delivery
With a relentless focus on precision and timeliness, we deliver your product on schedule, every time.
Coupled with post-project support, PRONAV remains your trusted partner throughout the process.
Our Proven 5-Stage Process to Success
We’ve perfected a five-stage process to streamline your clinical supply chain and deliver consistent results.
With an industry-leading 99.3% on-time delivery rate over the past 12 months, PRONAV Clinical ensures reliable, seamless support across every trial we serve.
Navigating the complex regulatory and quality landscape can be overwhelming, especially for emerging pharma and biotech companies in preclinical or Phase 1 stages. Mistakes in supply chain management or quality oversight can result in costly delays or the loss of irreplaceable drug products.
At PRONAV Clinical, we specialize in helping early-stage biotech and pharma innovators navigate supply chain complexities swiftly and safely. With a collaborative, boutique approach, we forecast and address challenges before they arise.
Unlike larger providers, we are committed to supporting even the smallest batch sizes, ensuring no project or medicine is overlooked - particularly for critical or rare disease treatments.
With bases in Ireland, and Maryland, USA, we seamlessly access European and US markets to ensure compliance, accessibility, and timely delivery for clinical trials worldwide.
Don’t risk the safety or integrity of your next-generation therapeutic.
1
PRONAV Consulting & Project Management
PRONAV’s foundation lies in the hands-on, consultative expertise we provide to our clients. We act as an extension of your team, creating bespoke roadmaps and offering project management to ensure your product’s on-time delivery.
-
Custom Process Flow Design: Built into our proprietary PROMAP platform for seamless document management.
-
End-to-End Project Management: From batch certification and release to supply chain auditing and due diligence, our qualified team has you covered.
-
Expert Guidance: Comprehensive support for ancillary medicine and medical device sourcing
2
Certifications
PRONAV Clinical holds Manufacturing and Importation Authorisations (MIAs) issued by the Health Products Regulatory Authority of Ireland for:
-
Investigational Medicinal Products (Authorisation #: IMP12681)
-
Commercial Human Medicinal Products (Authorisation #: M12679)
3
PRONAV Labelling, Storage & Shipment
PRONAV Clinical doesn’t just manage projects—we deliver them. With our specialized facility in Ireland, we offer in-house:
-
Post-Freeze Labelling for drug products stored at -80°C, enabling site-specific customization.
-
Comprehensive Packaging, Storage, and Shipping: Controlled-temperature solutions for any dosage form.
Real Results with PRONAV Clinical
Whether you’re producing 10 vials or 1,000 vials, PRONAV’s bespoke solutions and global reach ensure your product’s safety, compliance, and on-time delivery. We’re your single expert partner, dedicated to accelerating your journey to clinical trials.
Delivery Through Speed, Precision, and Bespoke Solutions
Speed:
Rapid response times and dynamic problem-solving ensure your timelines are met.
Precision:
Deep regulatory knowledge guarantees compliance and safety at every step.
Solutions-Driven:
Fully bespoke roadmaps and processes tailored to your specific needs.
PRONAV offers true end-to-end solutions, managing every step from project planning to labelling, storage, and shipping of final product.