You will get Professional SOP Review & Process Documentation Optimization

Irene G.Status: Offline
Irene G.

Let a pro handle the details

Buy Technical Writing services from Irene, priced and ready to go.
Irene G.Status: Offline
Irene G.

Let a pro handle the details

Buy Technical Writing services from Irene, priced and ready to go.

Project details

This service is designed for companies that already have SOPs but need them reviewed and improved for clarity and usability.
I will review your existing SOP documents and transform them into a clear, consistent, and professional set that is easy to read, navigate, and maintain. The focus is not on creating new procedures from scratch, but on improving what you already have.
This project includes:
 • Review of up to 3 existing SOPs
 • Structural and logical improvement (flow, clarity, consistency)
 • Standardization of formatting, headers, numbering, and layout
 • Alignment of documents into a single, coherent structure
 • Practical comments and recommendations for further improvement
I regularly work with large SOP libraries and quality systems where documents require restructuring rather than rewriting. My approach is systematic and focused on making procedures practical, readable, and usable by real teams.
This service is ideal if your SOPs feel fragmented, outdated, or difficult to follow.
Note: This service focuses on document structure, clarity, and usability. Regulatory compliance assessment or full system redesign can be provided as a separate service if required.
Document Type
Documentation
Topic
Manufacturing, Medical, Technology, General
Language
English, Russian, Other
What's included
Service Tiers Starter
$120
Standard
$250
Advanced
$420
Delivery Time 3 days 7 days 10 days
Number of Revisions
123
Consultation
Proofreading & Editing
Additional Research
-
-
References & Citations
-
-
-
Formatted Style Guide
-
Optional add-ons You can add these on the next page.
Fast Delivery
+$89
Additional Revision
+$50
Additional Research (+ 2 Days)
+$75
Irene G.Status: Offline

About Irene

Irene G.Status: Offline
Quality&Regulatory Compliance Consultant, Audits, ISO 13485, GDP
Trubia, Spain - 10:03 pm local time
I am a Quality & Regulatory Compliance Consultant with 15+ years of experience in pharmaceutical and medical device quality systems, audits, and regulatory oversight.

My background combines hands-on industry work and regulatory authority experience, including senior roles within the Ukrainian State Medicines Service, where I led investigations of substandard and falsified medicines and conducted audits in high-risk cases impacting patient safety.

I help companies to:
-build and improve Quality Management Systems (QMS)
- prepare for internal, supplier, and regulatory audits
- manage risk, deviations, CAPA, and change control
- develop clear, practical procedures and quality documentation
- ensure compliance with ISO 9001, GMP, GDP, and regulatory requirements
I am known for a pragmatic, risk-based approach, clear documentation, and the ability to work with complex cases where quality and patient safety are critical.
If you need a reliable expert who understands both regulatory expectations and real-world implementation, I would be glad to support your project.

Steps for completing your project

After purchasing the project, send requirements so Irene can start the project.

Delivery time starts when Irene receives requirements from you.

Irene works on your project following the steps below.

Revisions may occur after the delivery date.

Review & Initial Assessment

I review your existing SOPs to understand structure, clarity, consistency, and usability, identifying areas that need improvement.

Optimization & Structuring

I improve document structure, flow, formatting, headings, numbering, and alignment to create a clear and professional SOP set.

Review the work, release payment, and leave feedback to Irene.