You will get RP-HPLC Method Development & Validation

Dr Praveen K.Status: Offline
Dr Praveen K.

Let a pro handle the details

Buy Other Consulting & HR services from Dr Praveen, priced and ready to go.
Dr Praveen K.Status: Offline
Dr Praveen K.

Let a pro handle the details

Buy Other Consulting & HR services from Dr Praveen, priced and ready to go.

Project details

I provide professional RP-HPLC method development and validation services for pharmaceutical, academic, and research applications. With a PhD in Pharmaceutical Chemistry and strong hands-on experience in analytical method development, I help clients develop accurate, precise, and regulatory-compliant methods as per ICH guidelines.
My service includes complete method development, optimization, validation, data interpretation, and documentation for assay, impurity profiling, dissolution, and stability studies. I focus on achieving good resolution, peak symmetry, robustness, and reproducibility so that your method is suitable for publication, thesis submission, or regulatory use.
I have worked extensively on antidiabetic, cardiovascular, and other pharmaceutical compounds, and I understand both academic and industry expectations. You will receive clear chromatograms, validated results, and well-structured reports with scientific interpretation.
If you are a PhD scholar, M.Pharm student, researcher, or startup, I will support you step-by-step from concept to final validated method with complete confidentiality and professionalism.
What's included
Service Tiers Starter
$150
Standard
$300
Advanced
$600
Delivery Time 3 days 7 days 15 days
Number of Revisions
223

Frequently asked questions

Dr Praveen K.Status: Offline

About Dr Praveen

Dr Praveen K.Status: Offline
Research Consultant | HPLC & UV Method Development, Validation ICH(Q2)
Dehra Dun, India - 9:14 pm local time
Pharmaceutical Research Consultant | HPLC & UV Method Development and Validation Expert
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.

Understanding project scope and requirements

I review the drug details, analytical objective, regulatory requirements, and available data to clearly define the method development and validation strategy.

Method development and optimization

I develop and optimize chromatographic conditions including mobile phase, column selection, flow rate, and detection wavelength to achieve good resolution and peak shape.

Review the work, release payment, and leave feedback to Dr Praveen.