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Certificate Service

Service Provider of a wide range of services which include Free Sale Certification Service, BRC Certification Consultants Service, IATF 16949:2016 - Quality System For Automotive Industry, Sa 8000 Certification Services, Nabh Certification Service and Production Capacity Certificate Service.

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Free Sale Certification Service

₹ 5,000/CertificateGet Latest Price

Service TypeFree Sale Certification Service
Mode Of ServiceOnline
Duration10 Days
LocationIndia

A Free Sale Certificate (FSC) — also known as a Certificate of Free Sale, Certificate to Foreign Government (CFG), or Export Certificate — is an official document issued by a government authority (like the USFDA, Health Canada, or similar bodies) that states a product is freely sold and legally marketed in the country of origin.

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  • BRC Certification Consultants Service
  • BRC Certification Consultants Service
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BRC Certification Consultants Service

₹ 5,000/CertificateGet Latest Price

Service LocationIndia
Payment ModeOnline/Offline
Service ModeOnline
Delivery Time7 Days
Warranty1 Year

Certified Trainers with Industry Expertise
Practical, Case-Based Learning
  • On-Site, Online, and Hybrid Training Options
  • IRCA and NABCB Approved Courses (Where applicable)
Certificate of Completion for all Participants
Custom Programs for Medical, Pharma, Manufacturing & IT Industries
Section 3: ISO Standards We Cover
  • ISO Standard Training Offered
  • ISO 9001:2015 QMS – Lead Auditor, Internal Auditor, Awareness
  • ISO 13485:2016 Medical Device QMS – Internal/Lead Auditor
  • ISO 14001:2015 EMS – Environmental Management
  • ISO 45001:2018 OHSMS – Occupational Health & Safety
  • ISO 22000:2018 Food Safety Management
  • ISO 27001:2022 Information Security Management
  • ISO 17025:2017 Lab Competency & Calibration
  • ISO 50001:2018 Energy Management SystemGMP & Regulatory Training EU, WHO-GMP, USFDA, CDSCO
Section 4: Types of Training Programs
  • Lead Auditor Training (5 Days)Internationally recognized course for professionals aiming to conduct or lead third-party audits.
  • Internal Auditor Training (2 Days)Ideal for QA/QC staff, supervisors, and managers performing internal audits.
  • Awareness Training (1 Day)Basic overview of ISO clauses, structure, and implementation strategy for employees.
  • Customized Corporate TrainingTailored programs specific to your operations, SOPs, and compliance requirements.
Section 5: Who Should Attend?Quality Managers & Executives
  • Regulatory Affairs Professionals
  • Production/Engineering Staff
  • Medical Device, Pharma, and Hospital Personnel
  • Business Owners & Consultants

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  • IATF 16949:2016 - Quality System For Automotive Industry
  • IATF 16949:2016 - Quality System For Automotive Industry
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Service LocationIndia
Payment ModeOnline Offline
Delivery Time7 Days
Service ModeOnline/Offline
Warranty1 Year

Certified Trainers with Industry Expertise
Practical, Case-Based Learning
  • On-Site, Online, and Hybrid Training Options
  • IRCA and NABCB Approved Courses (Where applicable)
Certificate of Completion for all Participants
Custom Programs for Medical, Pharma, Manufacturing & IT Industries
Section 3: ISO Standards We Cover
  • ISO Standard Training Offered
  • ISO 9001:2015 QMS – Lead Auditor, Internal Auditor, Awareness
  • ISO 13485:2016 Medical Device QMS – Internal/Lead Auditor
  • ISO 14001:2015 EMS – Environmental Management
  • ISO 45001:2018 OHSMS – Occupational Health & Safety
  • ISO 22000:2018 Food Safety Management
  • ISO 27001:2022 Information Security Management
  • ISO 17025:2017 Lab Competency & Calibration
  • ISO 50001:2018 Energy Management SystemGMP & Regulatory Training EU, WHO-GMP, USFDA, CDSCO
Section 4: Types of Training Programs
  • Lead Auditor Training (5 Days)Internationally recognized course for professionals aiming to conduct or lead third-party audits.
  • Internal Auditor Training (2 Days)Ideal for QA/QC staff, supervisors, and managers performing internal audits.
  • Awareness Training (1 Day)Basic overview of ISO clauses, structure, and implementation strategy for employees.
  • Customized Corporate TrainingTailored programs specific to your operations, SOPs, and compliance requirements.
Section 5: Who Should Attend?Quality Managers & Executives
  • Regulatory Affairs Professionals
  • Production/Engineering Staff
  • Medical Device, Pharma, and Hospital Personnel
  • Business Owners & Consultants

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  • Sa 8000 Certification Services
  • Sa 8000 Certification Services
  • Sa 8000 Certification Services
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Sa 8000 Certification Services

₹ 5,000/CertificateGet Latest Price

Service LocationIndia
Payment ModeOnline/Offline
Service ModeOnline
Delivery Time7 Days
Warranty1 Year

Certified Trainers with Industry Expertise
Practical, Case-Based Learning
  • On-Site, Online, and Hybrid Training Options
  • IRCA and NABCB Approved Courses (Where applicable)
Certificate of Completion for all Participants
Custom Programs for Medical, Pharma, Manufacturing & IT Industries
Section 3: ISO Standards We Cover
  • ISO Standard Training Offered
  • ISO 9001:2015 QMS – Lead Auditor, Internal Auditor, Awareness
  • ISO 13485:2016 Medical Device QMS – Internal/Lead Auditor
  • ISO 14001:2015 EMS – Environmental Management
  • ISO 45001:2018 OHSMS – Occupational Health & Safety
  • ISO 22000:2018 Food Safety Management
  • ISO 27001:2022 Information Security Management
  • ISO 17025:2017 Lab Competency & Calibration
  • ISO 50001:2018 Energy Management SystemGMP & Regulatory Training EU, WHO-GMP, USFDA, CDSCO
Section 4: Types of Training Programs
  • Lead Auditor Training (5 Days)Internationally recognized course for professionals aiming to conduct or lead third-party audits.
  • Internal Auditor Training (2 Days)Ideal for QA/QC staff, supervisors, and managers performing internal audits.
  • Awareness Training (1 Day)Basic overview of ISO clauses, structure, and implementation strategy for employees.
  • Customized Corporate TrainingTailored programs specific to your operations, SOPs, and compliance requirements.
Section 5: Who Should Attend?Quality Managers & Executives
  • Regulatory Affairs Professionals
  • Production/Engineering Staff
  • Medical Device, Pharma, and Hospital Personnel
  • Business Owners & Consultants

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Nabh Certification Service

₹ 5,000/CertificateGet Latest Price

Service LocationIndia
Target LocationState
Document verification ModeOffline
Service ModeOnline
Payment ModeOnline/Offline

Certified Trainers with Industry Expertise
Practical, Case-Based Learning
  • On-Site, Online, and Hybrid Training Options
  • IRCA and NABCB Approved Courses (Where applicable)
Certificate of Completion for all Participants
Custom Programs for Medical, Pharma, Manufacturing & IT Industries
Section 3: ISO Standards We Cover
  • ISO Standard Training Offered
  • ISO 9001:2015 QMS – Lead Auditor, Internal Auditor, Awareness
  • ISO 13485:2016 Medical Device QMS – Internal/Lead Auditor
  • ISO 14001:2015 EMS – Environmental Management
  • ISO 45001:2018 OHSMS – Occupational Health & Safety
  • ISO 22000:2018 Food Safety Management
  • ISO 27001:2022 Information Security Management
  • ISO 17025:2017 Lab Competency & Calibration
  • ISO 50001:2018 Energy Management SystemGMP & Regulatory Training EU, WHO-GMP, USFDA, CDSCO
Section 4: Types of Training Programs
  • Lead Auditor Training (5 Days)Internationally recognized course for professionals aiming to conduct or lead third-party audits.
  • Internal Auditor Training (2 Days)Ideal for QA/QC staff, supervisors, and managers performing internal audits.
  • Awareness Training (1 Day)Basic overview of ISO clauses, structure, and implementation strategy for employees.
  • Customized Corporate TrainingTailored programs specific to your operations, SOPs, and compliance requirements.
Section 5: Who Should Attend?Quality Managers & Executives
  • Regulatory Affairs Professionals
  • Production/Engineering Staff
  • Medical Device, Pharma, and Hospital Personnel
  • Business Owners & Consultants

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Production Capacity Certificate Service

₹ 5,000/CertificateGet Latest Price

Service TypeProduction Capacity Certificate Service
Mode Of ServiceOnline

A Production Capacity Certificate is an official document that certifies the maximum quantity of products a manufacturing facility can produce within a specific time frame (monthly or annually). It is typically issued by a Chartered Engineer (CE), Industry Associations, or sometimes government authorities depending on the country and industry.

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  • Isi Mark Certification Services
  • Isi Mark Certification Services
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Isi Mark Certification Services

₹ 5,000/CertificateGet Latest Price

Service LocationIndia
Service ModeOnline
Payment ModeOnline/ Offline
Delivery ModeOnline Offline
Warranty1 Year

Certified Trainers with Industry Expertise
Practical, Case-Based Learning
  • On-Site, Online, and Hybrid Training Options
  • IRCA and NABCB Approved Courses (Where applicable)
Certificate of Completion for all Participants
Custom Programs for Medical, Pharma, Manufacturing & IT Industries
Section 3: ISO Standards We Cover
  • ISO Standard Training Offered
  • ISO 9001:2015 QMS – Lead Auditor, Internal Auditor, Awareness
  • ISO 13485:2016 Medical Device QMS – Internal/Lead Auditor
  • ISO 14001:2015 EMS – Environmental Management
  • ISO 45001:2018 OHSMS – Occupational Health & Safety
  • ISO 22000:2018 Food Safety Management
  • ISO 27001:2022 Information Security Management
  • ISO 17025:2017 Lab Competency & Calibration
  • ISO 50001:2018 Energy Management SystemGMP & Regulatory Training EU, WHO-GMP, USFDA, CDSCO
Section 4: Types of Training Programs
  • Lead Auditor Training (5 Days)Internationally recognized course for professionals aiming to conduct or lead third-party audits.
  • Internal Auditor Training (2 Days)Ideal for QA/QC staff, supervisors, and managers performing internal audits.
  • Awareness Training (1 Day)Basic overview of ISO clauses, structure, and implementation strategy for employees.
  • Customized Corporate TrainingTailored programs specific to your operations, SOPs, and compliance requirements.
Section 5: Who Should Attend?Quality Managers & Executives
  • Regulatory Affairs Professionals
  • Production/Engineering Staff
  • Medical Device, Pharma, and Hospital Personnel
  • Business Owners & Consultants

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  • Rohs Certification Services
  • Rohs Certification Services
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Rohs Certification Services

₹ 5,000/CertificateGet Latest Price

Service LocationIndia
Certifications ProvidedROHS Certification Consultancy Services
Document verification ModeOnline
Mode of ReportSoft Copy
Service ModeOnline Offline

Certified Trainers with Industry Expertise
Practical, Case-Based Learning
  • On-Site, Online, and Hybrid Training Options
  • IRCA and NABCB Approved Courses (Where applicable)
Certificate of Completion for all Participants
Custom Programs for Medical, Pharma, Manufacturing & IT Industries
Section 3: ISO Standards We Cover
  • ISO Standard Training Offered
  • ISO 9001:2015 QMS – Lead Auditor, Internal Auditor, Awareness
  • ISO 13485:2016 Medical Device QMS – Internal/Lead Auditor
  • ISO 14001:2015 EMS – Environmental Management
  • ISO 45001:2018 OHSMS – Occupational Health & Safety
  • ISO 22000:2018 Food Safety Management
  • ISO 27001:2022 Information Security Management
  • ISO 17025:2017 Lab Competency & Calibration
  • ISO 50001:2018 Energy Management SystemGMP & Regulatory Training EU, WHO-GMP, USFDA, CDSCO
Section 4: Types of Training Programs
  • Lead Auditor Training (5 Days)Internationally recognized course for professionals aiming to conduct or lead third-party audits.
  • Internal Auditor Training (2 Days)Ideal for QA/QC staff, supervisors, and managers performing internal audits.
  • Awareness Training (1 Day)Basic overview of ISO clauses, structure, and implementation strategy for employees.
  • Customized Corporate TrainingTailored programs specific to your operations, SOPs, and compliance requirements.
Section 5: Who Should Attend?Quality Managers & Executives
  • Regulatory Affairs Professionals
  • Production/Engineering Staff
  • Medical Device, Pharma, and Hospital Personnel
  • Business Owners & Consultants

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  • Iatf 16949 2016 Certification Services
  • Iatf 16949 2016 Certification Services
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Iatf 16949 2016 Certification Services

₹ 5,000/CertificateGet Latest Price

Service LocationIndia
Service ModeOnline
Payment ModeOnline/offline
Delivery Mode1-7 Days
Service TypeLATF Service

Certified Trainers with Industry Expertise
Practical, Case-Based Learning
  • On-Site, Online, and Hybrid Training Options
  • IRCA and NABCB Approved Courses (Where applicable)
Certificate of Completion for all Participants
Custom Programs for Medical, Pharma, Manufacturing & IT Industries
Section 3: ISO Standards We Cover
  • ISO Standard Training Offered
  • ISO 9001:2015 QMS – Lead Auditor, Internal Auditor, Awareness
  • ISO 13485:2016 Medical Device QMS – Internal/Lead Auditor
  • ISO 14001:2015 EMS – Environmental Management
  • ISO 45001:2018 OHSMS – Occupational Health & Safety
  • ISO 22000:2018 Food Safety Management
  • ISO 27001:2022 Information Security Management
  • ISO 17025:2017 Lab Competency & Calibration
  • ISO 50001:2018 Energy Management SystemGMP & Regulatory Training EU, WHO-GMP, USFDA, CDSCO
Section 4: Types of Training Programs
  • Lead Auditor Training (5 Days)Internationally recognized course for professionals aiming to conduct or lead third-party audits.
  • Internal Auditor Training (2 Days)Ideal for QA/QC staff, supervisors, and managers performing internal audits.
  • Awareness Training (1 Day)Basic overview of ISO clauses, structure, and implementation strategy for employees.
  • Customized Corporate TrainingTailored programs specific to your operations, SOPs, and compliance requirements.
Section 5: Who Should Attend?Quality Managers & Executives
  • Regulatory Affairs Professionals
  • Production/Engineering Staff
  • Medical Device, Pharma, and Hospital Personnel
  • Business Owners & Consultants

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Tl 9000 Certification Services

₹ 5,000/CertificateGet Latest Price

ISO StandardISO 9001
Mode of ServiceOnline
WorkISMS Certification service
Payment modeOnline / offline

Certified Trainers with Industry Expertise
Practical, Case-Based Learning
  • On-Site, Online, and Hybrid Training Options
  • IRCA and NABCB Approved Courses (Where applicable)
Certificate of Completion for all Participants
Custom Programs for Medical, Pharma, Manufacturing & IT Industries
Section 3: ISO Standards We Cover
  • ISO Standard Training Offered
  • ISO 9001:2015 QMS – Lead Auditor, Internal Auditor, Awareness
  • ISO 13485:2016 Medical Device QMS – Internal/Lead Auditor
  • ISO 14001:2015 EMS – Environmental Management
  • ISO 45001:2018 OHSMS – Occupational Health & Safety
  • ISO 22000:2018 Food Safety Management
  • ISO 27001:2022 Information Security Management
  • ISO 17025:2017 Lab Competency & Calibration
  • ISO 50001:2018 Energy Management SystemGMP & Regulatory Training EU, WHO-GMP, USFDA, CDSCO
Section 4: Types of Training Programs
  • Lead Auditor Training (5 Days)Internationally recognized course for professionals aiming to conduct or lead third-party audits.
  • Internal Auditor Training (2 Days)Ideal for QA/QC staff, supervisors, and managers performing internal audits.
  • Awareness Training (1 Day)Basic overview of ISO clauses, structure, and implementation strategy for employees.
  • Customized Corporate TrainingTailored programs specific to your operations, SOPs, and compliance requirements.
Section 5: Who Should Attend?Quality Managers & Executives
  • Regulatory Affairs Professionals
  • Production/Engineering Staff
  • Medical Device, Pharma, and Hospital Personnel
  • Business Owners & Consultants

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  • Food Safety Certification Services
  • Food Safety Certification Services
  • Food Safety Certification Services
  • Food Safety Certification Services
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Food Safety Certification Services

₹ 5,000/YearGet Latest Price

Service LocationIndia
Food Safety Certification ServicesFood Safety License Service
Services ModeOnline and Offline
Type Of IndustryFood
Payment ModeOnline/Offline
Warranty1 Year

Food safety Managment system service  provides professional Quality Management solutions for ISO and Continual Process Improvement on product & Services. We can assist your company to achieve ISO & Product certification. We are a friendly and approachable company in management systems; and are experienced over a wide range of industries and business sectors.

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  • US FDA Registration Service
  • US FDA Registration Service
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US FDA Registration Service

₹ 5,000/CertificateGet Latest Price

Service ModeOnline
Service TypeUSFDA Registration Service
LocationWorld Wide
LanguageEnglish
Duration3 Month
Payment ModeOnline/Offline

Medical devices must be registered with the U.S. Food and Drug Administration (FDA), and depending on their device class, they may require:
Establishment Registration
Device Listing
510(k) Premarket Notification
De Novo or PMA (for high-risk devices)
UDI (Unique Device Identifier) compliance
Labeling as per 21 CFR Part 801
🧩 Our USFDA Compliance Services1️⃣ Establishment Registration (FDA Device Facility)Annual registration with FDA
US Agent appointment for non-U.S. companies
FURLS account setup and payment processing
2️⃣ Device ListingSubmission of product details via FDA's FURLS
Assignment of proprietary and classification names
GUDID (Global Unique Device Identification Database) submission
3️⃣ 510(k) Premarket NotificationRequired for most Class II devices
Preparation and submission of 510(k) dossier
Substantial equivalence analysis
Interaction with FDA reviewers
4️⃣ Technical Documentation SupportDevice Description
Indications for Use
Biocompatibility, Electrical Safety, Sterility Data
Risk Management (ISO 14971) & Clinical Evaluation
5️⃣ Label Review & UDI ComplianceLabel format as per FDA 21 CFR Part 801
UDI (GS1/HIBCC), barcode generation, and packaging compliance
🔍 Device Classification (USFDA)Class Risk Level Pathway ExamplesClass I Low Risk Exempt or General Controls Surgical gloves, tongue depressorsClass II Moderate Risk 510(k) Premarket Notification Syringes, catheters, IVDsClass III High Risk PMA or De Novo Heart valves, implantable devices
🌐 Why Choose [Your Company Name]?✅ Experience with 100+ USFDA device registrations
✅ Support for Indian and international manufacturers
✅ Affordable U.S. Agent services
✅ Fast, transparent, and compliant processes
✅ Dedicated technical and regulatory team

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Non Conventional Certificate Service

₹ 5,000/PieceGet Latest Price

Service TypeNon Convectional Certificate Service
Mode Of ServiceOffline

A Non-Conventional Certificate generally refers to a certification or approval process for products, systems, or companies involved in renewable or non-conventional energy sources, such as:

  • Solar energy

  • Wind power

  • Biomass

  • Small hydro projects

  • Waste-to-energy systems

 

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C PAT Certification

₹ 5,000/CertificateGet Latest Price

Service LocationIndia
Service ModeOnline/Offline
Payment ModeOnline Offline
Delivery Mode7 Days
Warranty1 Year

Certified Trainers with Industry Expertise
Practical, Case-Based Learning
  • On-Site, Online, and Hybrid Training Options
  • IRCA and NABCB Approved Courses (Where applicable)
Certificate of Completion for all Participants
Custom Programs for Medical, Pharma, Manufacturing & IT Industries
Section 3: ISO Standards We Cover
  • ISO Standard Training Offered
  • ISO 9001:2015 QMS – Lead Auditor, Internal Auditor, Awareness
  • ISO 13485:2016 Medical Device QMS – Internal/Lead Auditor
  • ISO 14001:2015 EMS – Environmental Management
  • ISO 45001:2018 OHSMS – Occupational Health & Safety
  • ISO 22000:2018 Food Safety Management
  • ISO 27001:2022 Information Security Management
  • ISO 17025:2017 Lab Competency & Calibration
  • ISO 50001:2018 Energy Management SystemGMP & Regulatory Training EU, WHO-GMP, USFDA, CDSCO
Section 4: Types of Training Programs
  • Lead Auditor Training (5 Days)Internationally recognized course for professionals aiming to conduct or lead third-party audits.
  • Internal Auditor Training (2 Days)Ideal for QA/QC staff, supervisors, and managers performing internal audits.
  • Awareness Training (1 Day)Basic overview of ISO clauses, structure, and implementation strategy for employees.
  • Customized Corporate TrainingTailored programs specific to your operations, SOPs, and compliance requirements.
Section 5: Who Should Attend?Quality Managers & Executives
  • Regulatory Affairs Professionals
  • Production/Engineering Staff
  • Medical Device, Pharma, and Hospital Personnel
  • Business Owners & Consultants

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