INSIGHT OF OUR QUALITY MANAGEMENT , REGULATORY AFFAIRS AND GMPCONSULTING SERVICESBy:J.Ramniwas(M.Sc , M.Phil –Medicinal Ch...
2Gateway to Global compliance with a promiseWe are one of the leading Regulatory Affairs and Quality ManagementService Pro...
3• Name: J.Ramniwas(International Speaker,Writer,Auditor and Technical, Scientific and Regulatory Affairs Advisor)• Qualif...
4• His experience includes Regulatory Affairs, Analytical Development,Analytical Validations, Quality Control, Quality Ass...
5• He is a member of Drug Information Association (DIA), IndianPharmaceutical Association• He is also making contribution ...
6Sai Pharma Solutions Inc is a boutique consultancy tothe pharmaceutical industries dealing in1. API Manufacturing2. Drug ...
7PreparingPreparing PharmaceuticalPharmaceutical Industries/InstitutesIndustries/Institutes forfor GlobalGlobalRegulatoryR...
81. MakingMaking PharmaceuticalPharmaceutical Industries/Industries/ InstitutesInstitutes appreciateappreciate thethe need...
9Regulatory Approval Requires:1. Qualified Facilities2. Qualified Equipments ,Instruments and Utilities3. Qualified Method...
10What We Offer……?What We Offer……?1. ProvidingProviding consultingconsulting andand resourcesresources forfor validationva...
11Our Team IncludesOur Team Includes1.Regulatory Affairs Consultants2. Professional Trainers3. Validation Consultants4. Ph...
12We undertake GAP analysis for the following activities:1. Design Support for the upcoming manufacturing facilities.2. Ne...
13We undertake Audit services and provide checklists for :1. Internal Audits2. Third Party Audits for Vendor Qualification...
14We identify SOPs as per your business module, preparethem and impart training prior to their implementation:1. System SO...
15We conduct following trainingWe conduct following training programs but not limited to:programs but not limited to:••CFR...
16We offer the following documentation services but not limited to:We offer the following documentation services but not l...
17We undertake the following validation and qualification services.We execute validation and qualification activities as p...
18RegulatoryRegulatory ServicesServices areare thethe cornercorner stonestone toto thethe businessbusiness successsuccess....
19WeWe extendextend supportsupport inin regulatoryregulatory documentdocument preparation,preparation, review,review,submi...
20WeWe tackletackle youryour scientificscientific andand technicaltechnical queriesqueries pertainingpertaining totoregula...
21We extend support both the vendors and customers for businessdevelopment through a strategic alliance and agreements. We...
22Our company is the first pharmaceutical GMP consulting service provider in India to bebased entirely on the Internet. We...
23There are many reasons that you get associated with us for all Regulatory Affairs,Quality and GMP compliance solutions. ...
24We have customers in various pharmaceutical fields in India and overseas to whomwe are providing our value added service...
25J.RAMNIWAS (International speaker,writer, auditor and Regulatory & QMS technical advisor)( Founder and CEO)102102,Shradd...
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Sai pharma solutions inc scientific-regulatory affairs-qms and c gmp consultants

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We are one of the leading Regulatory Affairs and Quality Management Service Providers and Consultants of India since 2008 with focus on Quality. We have rich and varied experience of extending support to pharmaceutical industries for GMP, Regulatory and Quality Compliance. Customer satisfaction is our guiding force. We aim at aligning our process with the needs of the customer. So that all we do revolves around what our customer’s needs are. No wonder, satisfied customers are our biggest strength. Our process driven approach helps us deliver what we promise. And foster the trust the name Sai Pharma Solutions evoke.
Our Motto: “Start to finish, everything in between”

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Sai pharma solutions inc scientific-regulatory affairs-qms and c gmp consultants

  1. 1. INSIGHT OF OUR QUALITY MANAGEMENT , REGULATORY AFFAIRS AND GMPCONSULTING SERVICESBy:J.Ramniwas(M.Sc , M.Phil –Medicinal Chemistry)Founder and CEOSai Pharma Solutions Inc, Vadodara(India)Sai Pharma Solutions Inc, Vadodara(India)
  2. 2. 2Gateway to Global compliance with a promiseWe are one of the leading Regulatory Affairs and Quality ManagementService Providers and Consultants of India since 2008 with focus on Quality.We have rich and varied experience of extending support to pharmaceuticalindustries for GMP, Regulatory and Quality Compliance. Customersatisfaction is our guiding force. We aim at aligning our process with theneeds of the customer. So that all we do revolves around what ourcustomer’s needs are. No wonder, satisfied customers are our biggeststrength. Our process driven approach helps us deliver what we promise.And foster the trust the name Sai Pharma Solutions evoke.Our Motto: “Start to finish, everything in between”
  3. 3. 3• Name: J.Ramniwas(International Speaker,Writer,Auditor and Technical, Scientific and Regulatory Affairs Advisor)• Qualification(s): M.Sc, M.Phil(Medicinal Chemistry)• Mr. J.Ramniwas has total more than 22 years of experience in variousPharmaceutical industries as Global Quality Management and RegulatoryAffairs Professional.• Mr.J.Ramniwas is the founder and Chief Executive Officer at Sai PharmaSolutions Inc. headquartered in Vadodara, India• He has been responsible for GMP compliance, Regulatory Affairs andQuality Management Compliance services to various clients of Sai PharmaSolutions Inc.• He has held various management positions in many pharmaceuticalorganizations such as Lupin Limited, Zandu, Zydus Cadila HealthcareLimited, Tonira Pharma Limited and Tonira Chemical Company Limited,Titan Laboratories Pvt Limited.Global Quality Management and Regulatory AffairsProfessional Profile -1
  4. 4. 4• His experience includes Regulatory Affairs, Analytical Development,Analytical Validations, Quality Control, Quality Assurance, Development andEstablishment of Quality Systems, GMP and Regulatory Affairs trainings,Qualifications and Validations of Facilities, Equipments and Utilities, GMPDocumentation, Auditing, Regulatory Submissions, Hosting customer andRegulatory Audits, Risk Management and Compliance to Global RegulatoryRequirements• Mr. J.Ramniwas has extensive experience of working with internationalregulatory agencies, international associations such as USFDA, HealthCanada, EDQM, Korean FDA, ISO, MHLW, Japan and DIA,WHO etc. andmultinational customers such as Sandoz, TEVA, Polpharma, Almiral,Astellas Torii, Nippon, Apotex, Corepharma Actavis, Takeda and DaichiSankyo etc.Global Quality Management and Regulatory AffairsProfessional Profile -2
  5. 5. 5• He is a member of Drug Information Association (DIA), IndianPharmaceutical Association• He is also making contribution for writing articles on burning issues inpharmaceuticals and his articles have been published by the ExpressPharma Pulse, Pharma Times, Pharma Bio World, Pharma Guide and in-techjournal• J.Ramniwas is representing India as a speaker and trainer for internationalseminars on GMP, Regulatory Affairs and Quality Management Programsconducted by IBC (Asia),Asia Business Forum, Malaysia, Singapore, HongKong and Thailand, Global Regulatory Summits organized by CPhI etc.Global Quality Management and Regulatory AffairsProfessional Profile -3
  6. 6. 6Sai Pharma Solutions Inc is a boutique consultancy tothe pharmaceutical industries dealing in1. API Manufacturing2. Drug Product Manufacturing3. Cosmetic Manufacturing4. Ayurvedic and Herbal Product Manufacturing5. Biological/ Biotechnological Product Manufacturing6. Medical device manufacturingWe consult and train on Regulatory , GMP , Quality compliance,Drug registration, validation, qualification and continuousimprovement of manufacturing process.IntroductionIntroduction
  7. 7. 7PreparingPreparing PharmaceuticalPharmaceutical Industries/InstitutesIndustries/Institutes forfor GlobalGlobalRegulatoryRegulatory ComplianceCompliance byby education,education, training,training, auditing,auditing,documentationdocumentation andand regulatoryregulatory submissionssubmissions byby wayway ofof generatinggeneratingawarenessawareness amongamong thethe pharmaceuticalpharmaceutical entrepreneursentrepreneurs regardingregardingthethe futurefuture coursecourse ofof thethe regulatoryregulatory mechanismmechanism andand increasingincreasingcustomerscustomers expectationsexpectations consequentialconsequential technicaltechnical upgradationupgradation forforpharmaceuticalpharmaceutical manufacturingmanufacturing facilitiesfacilities..Our Vision
  8. 8. 81. MakingMaking PharmaceuticalPharmaceutical Industries/Industries/ InstitutesInstitutes appreciateappreciate thethe needneed toto changechange andandprepareprepare aa systematicsystematic actionaction planplan forfor reviewingreviewing “Manufacturing“Manufacturing ActivitiesActivities andandQualityQuality Systems”Systems” visvis--aa--visvis traditionaltraditional approachapproach ofof prioritizingprioritizing marketingmarketing focusfocus..22.. ToTo provideprovide ComprehensiveComprehensive understandingunderstanding ofof globalglobal regulatoryregulatory guidelinesguidelines enablingenablingthethe pharmaceuticalpharmaceutical organizationsorganizations toto assessassess theirtheir shortcomingsshortcomings..33.. CreateCreate awarenessawareness aboutabout thethe minimumminimum basicbasic levellevel ofof productionproduction systemssystems ii..ee..manufacturingmanufacturing facilities,facilities, design,design, equipmentequipment andand qualityquality managementmanagement systemssystems likelikedocumentationsdocumentations andand controlscontrols etcetc..44.. ToTo generategenerate positivepositive outlookoutlook toto faceface thethe challengechallenge confidentlyconfidently ratherrather thanthan takingtakingthethe escapeescape routeroute ii..ee.. waitwait andand watchwatch policypolicy oror believebelieve in”in” WhateverWhatever willwill happenhappen totothethe othersothers willwill happenhappen toto me”me”..55.. GeneratingGenerating aa perfectperfect clarityclarity aboutabout thethe regulatoryregulatory impactimpact –– itsits positivepositiveinterpretationinterpretation andand approachapproach toto implementimplement thethe necessarynecessary changeschanges inin technologytechnologyandand businessbusiness plansplans..66.. DevelopingDeveloping anan insightinsight amongamong thethe PharmaceuticalPharmaceutical industries/institutesindustries/institutes toto preparepreparechallengeschallenges ofof GlobalizationGlobalization..Our MissionOur Mission
  9. 9. 9Regulatory Approval Requires:1. Qualified Facilities2. Qualified Equipments ,Instruments and Utilities3. Qualified Methods and Processes4. Qualified personnel5. Risk Assessment6. Registration and regulatory submissions7. Flawless DocumentationM/s. Sai Pharma Solutions has been catering above requirements of ouresteemed customers since 2008 .Goal is : Regulatory ApprovalGoal is : Regulatory Approval
  10. 10. 10What We Offer……?What We Offer……?1. ProvidingProviding consultingconsulting andand resourcesresources forfor validationvalidation andand qualificationqualification activitiesactivities2.2. ConsultingConsulting onon howhow toto combinecombine GMPGMP compliancecompliance withwith TotalTotal QualityQualityManagement(TQM)Management(TQM) andand continuouscontinuous improvementimprovement techniquestechniques..3.3. ConsultingConsulting onon GxPGxP compliancecompliance4.4. ConsultingConsulting onon QualityQuality ComplianceCompliance5.5. ConsultingConsulting onon RegulatoryRegulatory ComplianceCompliance6.6. TrainingTraining PeoplePeople inin Validation,Validation, GMPGMP Compliance,Compliance, Documentation,Documentation, ContinuousContinuousimprovementimprovement andand careercareer enhanceenhance trainingtraining inin RA,QA,QC,ADL,RA,QA,QC,ADL, Manufacturing,Manufacturing, IPRIPRetcetc..7.7. ConsultingConsulting onon USFDA,PMDA,Japan,USFDA,PMDA,Japan, EU,EU, EDQM,TGA,EDQM,TGA, MCC,MHRAMCC,MHRA andand RestRest ofof thetheworld(ROW)world(ROW) DrugDrug registrationregistrationWeWe tackletackle validation,validation, qualification,qualification, registration,registration, documentationdocumentation compliancecompliance andandContinuousContinuous improvementimprovement projectsprojects onon aa fixedfixed priceprice oror hourlyhourly raterate basisbasis..
  11. 11. 11Our Team IncludesOur Team Includes1.Regulatory Affairs Consultants2. Professional Trainers3. Validation Consultants4. Pharmaceutical Engineers5. R&D and F&D Experts6. GMP Consultants7. Quality Management Consultants8. Analytical Development and Validation Consultants
  12. 12. 12We undertake GAP analysis for the following activities:1. Design Support for the upcoming manufacturing facilities.2. New Manufacturing building and facilities3. New Laboratory Establishment4. Quality System Development and Implementation5. To meet global regulatory requirements6. Existing facilities for Quality System ImprovementWe Offer : GAP AnalysisWe Offer : GAP Analysis
  13. 13. 13We undertake Audit services and provide checklists for :1. Internal Audits2. Third Party Audits for Vendor Qualification3. Mock audits prior to Regulatory and Customer Audits4. Support for Audit Preparation5. Audit Checklists6. Master Document Check ListWe Offer : Audits and ChecklistsWe Offer : Audits and Checklists
  14. 14. 14We identify SOPs as per your business module, preparethem and impart training prior to their implementation:1. System SOPs2. General SOPs3. Cleaning and Sanitation SOPs4. Passivation SOPs5. Departmental SOPs : QA,QC, Personnel & Admin,Microbiology, Engineering, R&D and Warehouse etc.6. Validation and Qualification SOPs7. Operation and Calibration SOPs8. Preventive Maintenance SOPsWe Offer : Standard Operating ProceduresWe Offer : Standard Operating Procedures
  15. 15. 15We conduct following trainingWe conduct following training programs but not limited to:programs but not limited to:••CFRCFR 210210 && 211211••European PharmaceuticalEuropean Pharmaceutical••ASEAN Member Country RegulationsASEAN Member Country Regulations••Japanese Pharmaceutical RegulationsJapanese Pharmaceutical Regulations••QQ77 (For API manufacturer)(For API manufacturer)••Ayurvedic and Herbal Product ManufacturesAyurvedic and Herbal Product Manufactures••Cosmetic ManufacturesCosmetic Manufactures•• Pharmaceutical Educational InstitutesPharmaceutical Educational Institutes••On Job trainingOn Job training••Training to Departmental heads to certify as internal trainerTraining to Departmental heads to certify as internal trainer••Specialize training for QC, QA & ManufacturingSpecialize training for QC, QA & Manufacturing••GMP related topics / GuidelinesGMP related topics / Guidelines••(e.g. HVAC, water system qualification, OOS, SOP preparation, regulatory(e.g. HVAC, water system qualification, OOS, SOP preparation, regulatoryrequirements while Specification designing, Analytical method Validation, procedurerequirements while Specification designing, Analytical method Validation, procedurevalidation etc)validation etc)•• Career enhancement trainingCareer enhancement trainingWe conduct inWe conduct in--house/ indoor/ outdoor training programmes. We also train thehouse/ indoor/ outdoor training programmes. We also train thetrainers internationally.trainers internationally.We Offer : Training and Development ProgramsWe Offer : Training and Development Programs
  16. 16. 16We offer the following documentation services but not limited to:We offer the following documentation services but not limited to:1.1. Site Master File( As per WHO/EUSite Master File( As per WHO/EU--GMP/PIC/s requirements)GMP/PIC/s requirements)2.2. Validation Master Plan(VMP)Validation Master Plan(VMP)3.3. Quality ManualQuality Manual4.4. Specifications and Analytical Procedures as per Regulatory RequirementSpecifications and Analytical Procedures as per Regulatory Requirement5.5. Master Production and Control Record(MPCR)Master Production and Control Record(MPCR)6.6. Batch Production and Control Record(BPCR)Batch Production and Control Record(BPCR)7.7. Validation Activities( Process Validation, Cleaning Validation, Analytical Method ValidationValidation Activities( Process Validation, Cleaning Validation, Analytical Method Validationetc.)etc.)8.8. Qualification of Equipments, instruments and utilities( URS,DQ,FAT,SAT,IQ,OQ and PQ) asQualification of Equipments, instruments and utilities( URS,DQ,FAT,SAT,IQ,OQ and PQ) asper ISPE guidelinesper ISPE guidelines9.9. Preventive Maintenance ChecklistsPreventive Maintenance Checklists10.10. Quality and GMP records and reportsQuality and GMP records and reports11.11. MSDS design as per REACH complianceMSDS design as per REACH compliance12.12. Genotoxic Impurities and Polymorphism StudyGenotoxic Impurities and Polymorphism Study13.13. Environment, Health and Safety(EHS) documentationEnvironment, Health and Safety(EHS) documentation14.14. API and Impurity characterization and structural elucidationAPI and Impurity characterization and structural elucidation15.15. Process/ Product Development Report( PDR)Process/ Product Development Report( PDR)16.16. Technology Transfer DocumentationTechnology Transfer Documentation17.17. Chemist/ Analyst ValidationChemist/ Analyst ValidationWe Offer : Documentation ServicesWe Offer : Documentation Services
  17. 17. 17We undertake the following validation and qualification services.We execute validation and qualification activities as per the pre-approved protocol and compile the report based on theobservations and findings. Protocol is also designed andprepared by us:1. Process Validation2. Cleaning Validation3. Analytical Method Development4. Analytical Method Validation5. Equipment/ Instrument Qualification( URS, DQ,FAT,SAT, IQ, OQ, PQ and MQ)6. Facility Qualification7. Utility Qualification8. Risk Assessment9. Successful Technology TransferWe Undertake : Validation and QualificationWe Undertake : Validation and Qualification
  18. 18. 18RegulatoryRegulatory ServicesServices areare thethe cornercorner stonestone toto thethe businessbusiness successsuccess.. WeWe offerofferfollowingfollowing regulatoryregulatory affairsaffairs servicesservices toto ensureensure youryour businessbusiness forayforay inin toto thetheregulatedregulated marketsmarkets::1.1. TechnicalTechnical DataData PackagePackage forfor APIs/APIs/ Intermediates/Intermediates/ StartingStarting MaterialsMaterials2.2. DrugDrug MasterMaster FilesFiles inin CTD/CTD/ ACTD/ACTD/ ee--CTDCTD // countrycountry specificspecific formatformat3.3. DrugDrug ProductProduct DossierDossier inin CTD,CTD, ACTD,ACTD, ee--CTDCTD oror countrycountry specificspecific formatsformats4.4. DocumentDocument ReviewReview5.5. FacilityFacility // ProductProduct Registration/Registration/ SiteSite AccreditationAccreditation etcetc..6.6. RegulatoryRegulatory SubmissionsSubmissions7.7. ResponseResponse toto regulatoryregulatory andand customercustomer queriesqueries8.8. DueDue diligencediligence9.9. AnnualAnnual UpdatesUpdates10.10.Amendment/Amendment/ VariationVariation FilingFilingWe Offer: Regulatory Affairs ServicesWe Offer: Regulatory Affairs Services
  19. 19. 19WeWe extendextend supportsupport inin regulatoryregulatory documentdocument preparation,preparation, review,review,submissionsubmission andand registrationregistration ofof drugsdrugs andand approvalapproval ofof facilitiesfacilitiesforfor::1.1. SiteSite Accreditation/RegistrationAccreditation/Registration2.2. ProductProduct RegistrationRegistration3.3. ScheduleSchedule ––MM GMPGMP4.4. StateState GMP(IssuedGMP(Issued byby thethe FDCAFDCA ofof statesstates ofof IndianIndian union)union)5.5. WHOWHO ––GMPGMP CertificationCertification6.6. COS/CEPCOS/CEP grantinggranting andand supportsupport inin hostinghosting EDQMEDQM inspectioninspection7.7. USPUSP VerificationVerification forfor APIsAPIs andand ExcipientsExcipients8.8. EUEU GMP/GMP/ CEPCEP--EDQM/EDQM/ USFDA/USFDA/ PMDA,PMDA, Japan/Japan/ MHRA,UK/MCCMHRA,UK/MCC ,, SouthSouthAfrica/TGAAfrica/TGA andand RestRest ofof thethe World(ROW)World(ROW)9.9. ISOISO--90019001--20082008 andand ISOISO--1400014000 DocumentationDocumentation SupportSupport10.10.NABLNABL AccreditationAccreditation11.11.REACHREACH ComplianceCompliance MSDSMSDS andand LabelLabel DesignDesignWe Offer: Approval and Accreditation SupportWe Offer: Approval and Accreditation Support
  20. 20. 20WeWe tackletackle youryour scientificscientific andand technicaltechnical queriesqueries pertainingpertaining totoregulatory/regulatory/ GMP/GMP/ QualityQuality compliancecompliance::1. Facility Design Requirement2. Product Development3. QbD Documentation(PDR etc)4. Chemistry and Manufacturing Controls5. Product Quality and Safety Issues6. Contamination Issues7. Change Control Issues8. Deviation Issues9. Patent and IPR discussion10. Regulatory Discussion11. Equipment/ Instrument requirement12.Water System Requirement13. AHU/HVAC System requirement14.Unit Operation Discussion15. Compressed gas requirement discussion16. Product contact utility discussionWe Offer: Scientific and Technical Discussions
  21. 21. 21We extend support both the vendors and customers for businessdevelopment through a strategic alliance and agreements. We supportfor:1. Vendor Development2. Technical Data Package at the product development stage3. Impurity Standards4. Customer Development Samples5. Audit for Vendor QualificationWe Support in: Product and Business DevelopmentWe Support in: Product and Business Development
  22. 22. 22Our company is the first pharmaceutical GMP consulting service provider in India to bebased entirely on the Internet. We work closely with experienced and highly skilledprofessional GMP experts from around the world, allowing you to benefit from their wide-ranging knowledge and expertise. As a result, pharmaceutical companies no longer need tospend several thousands of dollars on conventional consulting services to gather GMP-related information.Our role is to find the right answers to your questions and provide advice as and when youneed it. We specialize in conducting GMP and quality reviews in both English and locallanguages for batch records, annual product reviews, investigations, complaints anddeviations, etc. We can also assist you in the creation of documentation such as master batchrecords and standard operating procedures (SOPs).We also provide key pharmaceutical document templates such as SOPs, master plans andtraining modules to support your daily cGMP affairs. What’s more, as an Internet-basedconsultancy, we don’t generate costly travel and hotel expenses. Instead, we focus entirely onthe task in hand – providing you and your company with precisely the advice ordocumentation you need in the most cost-effective manner.We Offer: Online ConsultancyWe Offer: Online Consultancy
  23. 23. 23There are many reasons that you get associated with us for all Regulatory Affairs,Quality and GMP compliance solutions. Some of them are enumerated below:1. Meeting set targets within stipulated timelines2. Compliance with Global Quality Standards.3. Proven Past Track Record4. Commitment to Quality and Timely deliverance.5. Interacting with the personnel on shop floor to resolve issues6. Qualified and Competitive team.7. Professional Excellence8. Quality at a Reasonable cost.9. Ready to face audits by worldwide Regulatory authorities.10. Conducting audits for European/ Japanese customers in accordance withEDQM/EMEA/PMDA requirements11. Outsourcing can reduce the overhead costsWhy Sai Pharma Solutions…..?Why Sai Pharma Solutions…..?
  24. 24. 24We have customers in various pharmaceutical fields in India and overseas to whomwe are providing our value added services on continuous basis. Our Indian customers:1. Titan Laboratories Private Limited 23. Amoli Organics Pvt Ltd2. Titan Pharma Pvt Limited 24. UBM India Limited3. Nivika Chemo Pharma Private Limited 25. Anamayee Pharmachem Pvt Ltd4. Suchem Laboratories 26. Danopharm Chemicals P Limited5. Suleshvari Pharma6. Dolphin Chem7. Anuh Pharma Limited8. Orex Pharma Private Limited9. Apex Healthcare Limited10. Great Pacific Export Limited11. Anan Drugs and Chem Limited12. Annamalai University13. Gujarat University14. Asia Business Forum15. IBC(Asia)16. Parul Institute of Pharmacy17. Isomatric Health Care Limited18. Adani Pharmachem Private Limited19. Benzo Petro International Limited ( Arch Pharmalabs Limited)20. SICART21. Zephyr Synthesis Private Limited22. Rubamin Limited(Pharma Division)***In addition to India, we have customers in South Asian countries and other parts of the world.***In addition to India, we have customers in South Asian countries and other parts of the world.Our Esteemed CustomersOur Esteemed Customers
  25. 25. 25J.RAMNIWAS (International speaker,writer, auditor and Regulatory & QMS technical advisor)( Founder and CEO)102102,Shraddha Saburi,,Shraddha Saburi,Narayan Gardens, VUDA Road, GotriNarayan Gardens, VUDA Road, Gotri --390021390021Vadodara (Gujarat) IndiaVadodara (Gujarat) IndiaEmail:Email: jramniwas@saipharmasolutions.comjramniwas@saipharmasolutions.comPhone No: +Phone No: +919558809128919558809128Website:Website: www.saipharmasolutions.comwww.saipharmasolutions.comContact us for business associationContact us for business association

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