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ISO 9000, 9001, 14001, 13485, 16949, 19011, AS 9000, TL 9100, FDA, GMP Turnkey Solution
Provide ISO 9000, 9001, 14001, 13485, 16949, 19011, AS 9000, TL 9100, FDA, GMP turnkey solution for product system certification
Turnkey Solution ISO 9001 GMP FDA Certification
Turnkey ISO 9000 or GMP-FDA certification service is the perfect solution for companies that have limited staff resources, suffer from time constraints, need a cost-effective solution, or ISO 9001 certification interfere with daily operations. In such a context, we offer Turnkey certification expertise if your organization wants to comply with the required International Standards in a specific industry:
Turnkey Solution ISO 9001 GMP FDA Compliance
To comply with the required International Standards in your industry, we offer an implementation service that follows a 5-step quality six sigma methodology: Gap assessment, quality management system upgrade, training, internal audit, and ISO 9000 certification audit. We will provide and generate all the required documentation to meet the requirements of the standard. The implementation usually involves streamlining and simplification of your operation to take full advantage of the benefits of the standard. We have consultants in almost all the different states, Canada, Mexico, France, Brazil and North Africa
Turnkey Solution ISO 9001 GMP FDA Approach
Through a series of on-site interviews, we study your work flows and tailor the quality manual including procedures, policies, work instructions, and records to reflect your operations and quality management system requirements. Check a sample of Quality Manual.
Our experts know how to satisfy the documentation requirements of the ISO Standards. We work side-by-side with you during your preparation for the ISO audit, guiding you through each step along the path to succeed in product and system certification. Our experience and expertise in ISO and GMP-FDA International Standards enable us to offer an economical, streamlined solution to assist you in obtaining ISO 9000, ISO 14000, ISO, 13485, ISO 19011, ISO 16949, AS 9100, TL 9000, and GMP-FDA certification.
Turnkey Solution ISO 9001 GMP FDA Implementation
- Plan your ISO implementation process
- Determine reasonable ISO project milestones
- Define documentation to be developed
- Clarify desk-audit tasks to be accomplished
- Allocate personnel to be assigned to ISO development
- Prepare your Quality and/or Environmental manual/procedures
- Tailor ISO documents to suit your specific operating processes
- Provides audit training to the management staff
- Provide resources to manage the implementation process of the 9001 Quality and/or 14001 Environmental Management System
Turnkey Solution ISO 9000 GMP FDA Time Delivery
Preparing the system documentation QA Manual is typically the most difficult and most important hurdle for organizations seeking ISO or GMP-FDA Registration. But, our Six Sigma approach is designed to accelerate the completion of your documentation with little or no impact to your daily operations, effectively saving you time and money. The duration of the project depends on the size and complexity of your organization, and the scope of the project.
We have partnered with Caliso Consulting to extend our network of experts not only in the USA but also in Canada, Mexico, France, Brazil and North Africa. Check our ISO GMP FDA Certification Success Stories
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Clients that our Xperts have helped!
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ISO CERTIFICATION GUARANTEE
We offer “Total Satisfaction Refund Policy” for all eConsulting services that you purchase from CompetitiveXpert. If for any reason you are not satisfied with our eBusiness services or one of our experts, we will refund you. We will not charge you for our remaining time, and we will discontinue our collaboration. We are proud of our achievement, and want to show it through the explicit satisfaction of the clients that we have helped.
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CUSTOMER TESTIMONIAL
"CompetitiveXpert experts are very down-to-earth. They know all the details about business plan. But, the most important thing is that they can work patiently with people at every level of the organization to set up a Qualitative business plan that meets the venture requirements. With their help ArtVoila! has successfully raised funding for the first two years of development.”
Stephane Cordier
CEO
Art For All
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