We help Life Science Company stay away from 483, Warning Letters and Data Integrity Issues. We are a leading CSV Consultant of India working all round the world Let us explore Mutually Beneficial area.Data Integrity issues are like Diabetes it is not hard to controlled diabetes by better life style (Data Integrity Issues by Better Compliance). If diabetes is not controlled well it can be source of many diseases and has the power to kill the person when combined with other disease attack. Now as full GMP 21 CFR part 211 and 201 slowly coming to computers Data Integrity issue has become like Diabetes. If not controlled it can harm ever where and it can be dangerous for Financial health of any company. We have seen 1/3rd or 1/4th of market cap erosion in 2-3 days time. Only way to control is to live controlled and better compliance life style and medication (Training in case of data Integrity from Good Trainer). Please start Independent Third party Audit of Data Integrity and Data Governance. It can help reduce 483 and warning letter by great amount. Some points from my Recent TV interview on CNBC, Ping TV network and Regulatory Day Meet with Expert panel.http://www.moneycontrol.com/news/business/special-videos-trends/fda-woes-pharma-companies-feel-the-us-fda-heat-2244209.html?classic=truehttps://www.youtube.com/watch?v=4mAeBZz2mRIhttps://www.youtube.com/watch?v=gBK7MV6bUVQ&t=1s http://pvchronicle.com/computer-systems-validation-training-kalpesh-r-vaghela/

We are reputed company of India. We cater to more than 75% top client of India most of them are with us since last six years.. We work in many part of the world and carry out software validation for the Pharma Plant, Medical Device Manufacturer, Biotech as well as Clinical Research Companies. We help them get regulatory approval from FDA, MHRA, ANVISA, MCC, TGA etc… We actively work with companies in USA, Europe, Middle East and China. We are expert in Training on subjects like Why Validation?, GAMP5, 21 CFR Part 11 Compliance, Risk Assessment . Reduce your CAPA, Change Control by more focus on the Quality Production and Training. I am in charge of New BusinessMarketing and SalesInternational businessKVS Technologies is a leading Quality Validation Company of India.Infra Control Systems is a Leading Automation Company/ International Compunter Systems (CSV) Validation and Calibration Services provider.1) Pharma Automation. PLC and SCADA Program and Its Modification2) Training to your staff for above matters as well as GAMP5 and 21 CFR Part 11 Compliance3) Humidity-Temp-Pressure Monitoring and Control Systems4) Online Data Logger as well as Portable Data Loggers for shipment and refer Van. 5) Software Validation of PLC/ SCADA/ BMS/ DCS/ ERP/ LIMS etc. We are considered to be no.1 quality validation company of India. 6) We are launching world best Electronic Batch Data recording system for Pharmaceutical industries. The same software can be used by all other manufacturing plant as well. 7) Calibration and Thermal-Humidity profiling. 8) All types of measuring Instruments, Sensor. 9) Patented Motor protection relays to Stop Motor burn out problem from Single Phase, Over Load, Lock rotor, Ground Fault etc.10) CSV, GAMP5, Data Integrity and 21 CFR part 11 compliance Training 11) 21 CFR part 11 Compliance Audit, Annex 11 Compliance Audit, GAP Analyses Data Integrity Audit and Risk Assessment

KVS Technologies (KVS) is a 14 year old leading automation and Compliance consultant group headed by Expert Trainer cum Consultant Mr Kalpeshkumar Vaghela & Mr S P Sapavidya having 34 Years experience in field of Pharmaceuticals and Automation. KVS has strong track record for Computer Systems Validation, GAP Assessment, Risk Management, Training and Remediation for USFDA –MHRA- Canadian FDA, WHO-TGA-ANVISA and more. The validation based on Critical thinking and risk base (CFR 211.68, GAMP5 and Annex11) is the most important feature. We help you in setting your process right by mapping (GxP process flow, SDLC Life Cycle and Data Life Cycle ) it properly first and then validating. We can be your Onsite and offsite CSV and Compliance Support. We can help you at each stage of GAP Assessment, CSV, Risk Mitigation, Remediation and Training to your staff. This is the same process which many company do after receipt of 483 and warning letter. We do it proactively as our client reputation means a lot to us. We can help you a lot in current situation when most Pharma Company are getting 483- Warning Letters on Data Integrity and CSV front. Prevention is always better then cure and less expensive also. Good CSV can help you Reduce CAPA, Change Control, Batch Recall and give all people (Patient- Share holder and staff) a good Peace of mind. Patient safety, Product Quality and Data Integrity is a key focus of Regulatory Audits. We are rated as 20 most Promising Pharma and Biotechnologies Solution Provider Company of India for the year 2015-16 and 2014-15 by CIO Review. In Validation Category there is only one entry and that is we. We were also selected for Power of Idea Best Business Idea contest pan India. Year 2015 CIO review Top 20 Pharma Solution provider http://www.cioreview.in/magazines/pharma-special-nov-2015/Year 2014 CIO review Top 20 Pharma Solution provider http://www.cioreview.in/magazines/Pharma-mazter/

We are CSV Consultant, Trainer, help in GAP Assessment, Risk Management and remediation. We have started training on Compliance, Data Integrity, 21 CFR PART 11 COMPLIANCE, ANNEX 11, Risk Assessment, GAMP5, CSV Deliverable, Cloud Validation.Online Live Webinar / Class room/ Corporate Training is conducted in India and Abroad to make it more cost effective. Countries where we often visit are USA, Canada, Europe, China, Middle East. Select client list include Major Pharma Companies of India and world Glenmark, Dr. Reddy's Lab, Lupin, Watson, Eisai, Cipla, Alembic, SUN Pharma, Fresenious Kabi, Rusan Pharma , Biocon, HCL Global, Wipro, MphesiS, Thermo Lab, Anton Paar, Sartorious, Thermo Fischer, and many more.. We have conducted many International Conference as well. Internationally Emerson Process management China. Horiba Scientific FranceMuscat Pharmacy,CigalahMorton groves USA Actavis Iceland etc.

AMBE Investment and Insurance ConsultantString team with 3 time MDRT AdvisorFinancial PlanningRetirement PlanningMediclaim, Top Up, Liability Insurance Children Education and Marriage PlanningExpert on Best and Cost Effective Term PlanMutual Fund InvestmentGold, Silver InvestmentRealty investmentExpert on Asset AllocationPension PlansULIPsGold InvestmentRealty InvestmentSavings Account with Debit card and 8% interest reinvested daily

It is a group dedicated to Motivation and Inspiration by our Sir Professor Diwakar Rawla. It is an institute Of leadership and training.We all were very impressed by teaching of our great sir. True drive to be something great was ignited by him. We all have grown multi fold after the course and regualr meet with him. This is not a job but I felt like adding this in my profile. Thank you so mych to Diwakar Rawla Sir.

Looking after Automation, Electronics , Instrumentation and Computer Systems. Also checking Data Quality, Inetrpreting it, Discussing with Client,Computer Back up and Check.

Implementation of improved Instrument quality system for Oil Exploration. Computer system and Data Back Up Check. Observation and daily check up and Calibration of routine operation.Worked at North- South America, Canada, Argentina, Venezuela, Trinidad & Tobaggo, Gabon, Congo,Noway,Singapore,Brunei, Vietnam, Iran, Dubai, Qatar etc. Executive QA - for ORG System Quality Inspection and check. Coordination of QA and QC programs and functions Implementation of company's first self-directed work teams resulting in a flat organization Planning, development, and direction of Quality programs.

I worked As Observer and Senior observer. Looking after Seismic Survey Electronics, computer and Instrumentation Systems

Service Engineer for PC and Super Mini computers called prime