You will get accurate, structured and validated pharmacovigilance data
Project details
I will provide accurate and organized pharmacovigilance support for MedDRA coding and adverse event classification, ICSR data entry, case assessment, and related safety data processing. My services include reviewing source documents, extracting relevant case information, processing data according to client-provided instructions and SOPs, performing quality checks, identifying missing or inconsistent information, and delivering the completed work in the required format. I focus on accuracy, consistency, confidentiality, and timely delivery while following the client’s specific requirements and workflow. Whether you need support with individual cases, medical terminology coding, safety data organization, or quality checking, I can assist with structured and reliable pharmacovigilance data processing.
Data Entry Type
Data Cleansing, Document Conversion, Word ProcessingData Entry Tool
Microsoft Excel, Microsoft Office, Microsoft WordWhat's included
| Service Tiers |
Starter
$10
|
Standard
$25
|
Advanced
$45
|
|---|---|---|---|
| Delivery Time | 2 days | 3 days | 4 days |
Number of Revisions | 2 | 5 | 10 |
Number of Hours of Work | 10 | 15 | 20 |
Formatting & Clean Up | |||
Graph & Table Creation | - | - | - |
Optional add-ons
You can add these on the next page.
Fast Delivery
+$5 - $15
Additional Revision
+$5
Extra Cases
(+ 1 Day)
+$10About Yash
Data Entry & Transcription Services | Data Curation, Art Curation
Beed, India - 12:57 am local time
pharmaceutical science and clear, structured documentation. I
specialize in translating technical medical data, pharmacology
concepts, and clinical findings into highly accurate, reader-friendly
content.
Additionally, my academic training has given me strong
attention to detail, making me highly proficient in pharmaceutical
data curation, document formatting, and pharmacovigilance data
entry (ADR logging and tracking).I am available for 20 hours per
week for remote part-time roles, freelance contracts and data
curation projects.
Steps for completing your project
After purchasing the project, send requirements so Yash can start the project.
Delivery time starts when Yash receives requirements from you.
Yash works on your project following the steps below.
Revisions may occur after the delivery date.
Receive client materials
Collect the source documents, case reports, templates, SOPs, and specific processing instructions from the client.
Review case information
Review the provided documents and identify relevant patient, reporter, drug, adverse event, medical history, and treatment information.