You will get a comprehensive Clinical Evaluation Report for Medical Device Development
You will get a comprehensive Clinical Evaluation Report for Medical Device Development
Project details
I will provide you with a comprehensive document to support Regulatory Approvals by both United States FDA and European Union. I will perform literature and database searches, review articles to extract relevant information, and summarize data from identified reports. I will work closely with your study team to ensure that the content and results in clinical documents are accurate and complete as required. I will perform appropriate documented quality control checks on medical writing deliverables. I am knowledgeable and experienced in the regulatory medical writing process. If you need something else related to regulatory affairs, message me before placing your order.
Topic
Biotechnology, Medical, ScienceLanguage
EnglishWhat's included
| Service Tiers |
Starter
$3,000
|
Standard
$4,000
|
Advanced
$5,000
|
|---|---|---|---|
| Delivery Time | 42 days | 56 days | 70 days |
Number of Revisions | 2 | 4 | 8 |
Consultation | |||
Proofreading & Editing | |||
Additional Research | |||
References & Citations | |||
Formatted Style Guide |
About Ruth
Medical Writer / Medical Editor / Peer Reviewer
Athens, United States - 7:48 am local time
Document Types:
1. Manuscripts for Journal Submissions.
2. STEM Thesis and/or Dissertations.
3. STEM Editing for Multilingual and English as a Second Language Writers.
4. Monographs.
5. White Papers.
6. Contact me with inquiries if Document Type is Not Listed above.
Steps for completing your project
After purchasing the project, send requirements so Ruth can start the project.
Delivery time starts when Ruth receives requirements from you.
Ruth works on your project following the steps below.
Revisions may occur after the delivery date.
I will gather requirements
Kindly provide your archived documents to help me launch a comprehensive literature search.
Deliver First Draft
I will send you a draft 1 for review. We'll schedule a meeting at your convenience to agree on tables and figures to be included in the document. At the meeting, I will present you data and facilitate technical discussion as needed.