What types of medical writing services do you provide?

I provide medical writing services covering clinical and regulatory documentation, medical device documentation and patient-facing materials. My services include document preparation, writing, review and editing, depending on project requirements.

What types of documents can you prepare?

I work with a range of clinical, regulatory and medical device documents, including Clinical Study Protocols, Clinical Study Reports (CSRs), Investigator’s Brochures, Development Safety Update Reports (DSURs), Clinical Evaluation Reports (CERs), Clinical Investigation Plans (CIPs), Informed Consent Forms (ICFs) and other study-related documentation.

Who do you work with?

I provide medical writing support to Contract Research Organisations (CROs), pharmaceutical and biotechnology companies, clinical trial sponsors, medical device manufacturers, clinical researchers and investigators.

Do you work with international clients?

Yes. I am available to collaborate with clients internationally, subject to project requirements and agreed working arrangements.

Can you support individual projects as well as ongoing collaborations?

Yes. I can provide support for individual document assignments as well as longer-term projects, depending on availability, scope and timelines.

Do you offer document review and editing?

Yes. I can support the review and editing of existing clinical and regulatory documentation, focusing on clarity, accuracy, consistency, structure and alignment with applicable requirements.

What information do you need to provide a project estimate?

To assess a project, I generally need information about the document type, project scope, expected deliverables, available source materials and required timeline. Additional details may be discussed depending on the nature of the assignment.

How do you ensure the quality of your work?

I follow a structured approach focused on scientific accuracy, clarity, consistency and attention to detail. My work is informed by relevant regulatory requirements, internationally recognised guidelines and applicable documentation standards.

How do you handle confidential project information?

I understand the importance of confidentiality when working with clinical and regulatory documentation. Project-related information is handled with appropriate care, and confidentiality arrangements can be agreed before work begins.

How can I request a quotation or discuss a project?

You can contact me by email at anna@annagredecka.com

Please include a brief description of your project, the type of documentation required and your expected timeline. I will review your enquiry and get back to you to discuss the next step.