Why we do it?
To help our clients improve the lives of patients...
How we do it?
...by providing services recognised for quality, value, and collaboration
Medical Writing
We support all of your document writing and quality review needs, whether it is for single documents or through a functional service provider engagement.
Medical Communications
We provide comprehensive medical communication solutions, from pre-clinical research through to real-world practice.
Clinical Trial Transparency
CTT is foundational to your company’s commitment to patient centricity and we can keep you fully compliant in this area.
Plain Language Services
We create different types of plain language materials in traditional (PDF), infographic, and video formats.
Clinical Trial Transparency
CTT is foundational to your company’s commitment to patient centricity and we can keep you compliant in this area.
Writing
Services
We can support all your document writing needs, whether it is for single documents or through a functional service provider engagement.
Plain Language Services
We create different types of plain language documents in traditional (PDF), infographic, and video formats.
Redaction and Anonymisation
We redact and anonymise documents of all types to meet regulatory requirements.
Regulatory
We support you at every stage of the product lifecycle, from early development through post-market regulatory compliance.
Pharmacovigilance
Our comprehensive pharmacovigilance (PV) services help you ensure patient safety, remain compliant, and maintain the integrity of your products.
Medical Devices
Our end-to-end assistance and medical device services help you achieve compliance with global regulations, from product conception through post-market surveillance.
Training
We empower professionals with the knowledge and skills required to increase their effectiveness and develop their careers in clinical research through assignment-based training by our experienced faculty.
Staffing Solutions
Utilise our local presence in India to get access to the local talent market to leverage strategic advantage.
Other Services
Contact us with any other opportunities to collaborate, especially related to technology, administrative tasks, and consulting.
Quality Review
We can increase the quality of clinical trial documents while accelerating drug approval timelines and reducing costs.
Administrative Services
Many of your administrative activities could be delivered more effectively by us.
Consulting
We provide regulatory consulting services in our areas of expertise, either alongside our operational services or as a standalone engagement.
Project
Management
Our robust project delivery approach is based on 4 Cs – Collaboration, Consistency, Clarity, and Continuous learning.
“Over the last year the Krystelis team authored several regulatory documents for us. From the start the Krystelis project manager was highly collaborative, proactive, and flexible. All deliverables were completed according to the agreed timelines, and we were very satisfied with the quality of the work. It has been a great experience working with the team at Krystelis and we look forward to our continued collaboration. I would highly recommend Krystelis to anyone who requires medical writing support.”
Head of Medical Writing, Small Biotech (US)
“I highly recommend Krystelis for their outstanding services and support in data transparency consulting and operations. Their approach is thorough, systematic and fit for purpose. I have full confidence in their ability to deliver exceptional results. Their professionalism, attention to detail, and commitment to client satisfaction make them an ideal partner for any organisation seeking top-notch services.”
Head of Plain Language Summaries, Top 5 Pharma (US)
“Krystelis has provided our Centre for Drug Development with advice regarding our trial registration process and results reporting process and the advantages and disadvantages of different registries. The team at Krystelis has a wealth of experience in data transparency and we value their insight and support.”
Medical Writing Manager, Cancer Research UK
“I’m happy with Krystelis’ technical expertise in all our collaborations. I find you and your staff proactive, capable of responding and dealing with problems right away and you always take the time to understand our business requirements, needs, and challenges. For me and my staff, Krystelis is a trusted provider.”
Head of Clinical Compliance, Mid-sized Pharma (EU)
“Krystelis have provided our Centre for Drug Development with advice regarding our trial registration process and results reporting process and the advantages and disadvantages of different registries. The team at Krystelis have a wealth of experience in data transparency and we value their insight and support.”
Medical Writing Manager, Cancer Research UK
