You will get HPLC Troubleshooting & Peak Optimization for Pharmaceutical Analysis
Project details
I provide end-to-end support in pharmaceutical analytical research, specializing in HPLC method development, method validation (as per ICH guidelines), and research manuscript preparation for academic and industry use.
My approach is strictly scientific, not generic writing. Each project begins with feasibility assessment, followed by logical method design, experimental planning, data interpretation, and structured documentation.
I work with APIs, formulations, and combination products, covering assay, impurity, dissolution, and stability-indicating methods. I also support thesis work, research papers, and regulatory-style validation reports.
What sets my service apart is clarity, honesty, and technical depth. I do not overpromise. If a project is not feasible within scope or timeline, I communicate it upfront.
My goal is long-term collaboration based on trust, quality, and scientific integrity.
My approach is strictly scientific, not generic writing. Each project begins with feasibility assessment, followed by logical method design, experimental planning, data interpretation, and structured documentation.
I work with APIs, formulations, and combination products, covering assay, impurity, dissolution, and stability-indicating methods. I also support thesis work, research papers, and regulatory-style validation reports.
What sets my service apart is clarity, honesty, and technical depth. I do not overpromise. If a project is not feasible within scope or timeline, I communicate it upfront.
My goal is long-term collaboration based on trust, quality, and scientific integrity.
What's included
| Service Tiers |
Starter
$30
|
Standard
$60
|
Advanced
$120
|
|---|---|---|---|
| Delivery Time | 2 days | 3 days | 5 days |
Number of Revisions | 1 | 2 | 3 |
Frequently asked questions
About Dr Praveen
Research Consultant | HPLC & UV Method Development, Validation ICH(Q2)
Dehra Dun, India - 8:29 am local time
I am a PhD scholar in Pharmaceutical Chemistry with strong expertise in analytical method development and validation using HPLC and UV spectroscopy as per ICH guidelines. I specialize in supporting research scholars, postgraduate students, and industry professionals in developing robust, accurate, and compliant analytical methods.
My core areas of work include: • HPLC and UV method development and validation (ICH Q2R1 / Q2R2)
• Assay, dissolution, and content uniformity method support
• Analytical data interpretation and troubleshooting
• Research design support (AQbD, DoE basics)
• Thesis, dissertation, and research paper technical guidance
I have hands-on experience in pharmaceutical and analytical chemistry research, with multiple publications in reputed journals. I understand both academic and industry expectations, which helps me deliver practical and reliable solutions.
If you are a research scholar, student, or professional looking for clear guidance, correct methodology, and technically sound results, I will be happy to support your work.
Let’s work together to make your research strong, accurate, and publishable.
Steps for completing your project
After purchasing the project, send requirements so Dr Praveen can start the project.
Delivery time starts when Dr Praveen receives requirements from you.
Dr Praveen works on your project following the steps below.
Revisions may occur after the delivery date.
Requirement Analysis & Feasibility Check
Review drug details, scope, and client expectations to confirm technical feasibility and define clear boundaries.
Method Development / Study Design
Design chromatographic conditions and experimental approach based on drug properties and guideline requirements.