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US Market entry support. US Market entry support. Call us for a free quote! We provide global regulatory, compliance, and validation consulting services to the pharmaceutical, biologics, diagnostics, and medical device industries. We are an organization with a focus on customer needs and benefits. Alta Consulting believes in developing efficient and cost-effective regulatory solutions by understanding clients’ needs and applying best practices. 510(k), IDE, and PMA. IND, NDA, and BLA. 21 CFR Part 11.

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US Market entry support. US Market entry support. Call us for a free quote! We provide global regulatory, compliance, and validation consulting services to the pharmaceutical, biologics, diagnostics, and medical device industries. We are an organization with a focus on customer needs and benefits. Alta Consulting believes in developing efficient and cost-effective regulatory solutions by understanding clients’ needs and applying best practices. 510(k), IDE, and PMA. IND, NDA, and BLA. 21 CFR Part 11.

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1 medical devices

2 in vitro diagnostics

3 pharmaceuticals

4 biologics

5 blood/tissue

6 regulatory submissions

7 quality system

8 validations

9 software compliance

10 us agent services

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medical devices,in vitro diagnostics,pharmaceuticals,biologics,blood/tissue,regulatory submissions,quality system,validations,software compliance,us agent services,online document control,online capa system,info@altaconsulting us,validation service

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https://altaq.com

US Market entry support. US Market entry support. Call us for a free quote! We provide global regulatory, compliance, and validation consulting services to the pharmaceutical, biologics, diagnostics, and medical device industries. We are an organization with a focus on customer needs and benefits. Alta Consulting believes in developing efficient and cost-effective regulatory solutions by understanding clients’ needs and applying best practices. 510(k), IDE, and PMA. IND, NDA, and BLA. 21 CFR Part 11.

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http://www.altaq.com/Pharmaceuticals.html

US Market entry support. Call us for a quote! Team has successfully completed projects in Europe, Japan, SouthAsia, and China. We believe in providing efficient solutions in an effective manner. Our mission is to serve successful solutions. Regulatory Approvals (FDA and Europe). We have enabled our clients to successfully obtain regulatory approvals in the USA and Europe. Our services cover various aspects of regulatory submission depending on your needs. Regulatory Strategy and Planning. Our validation ...

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http://www.altaq.com/services.html

US Market entry support. US Market entry support. Call us for a free quote! Clients trust Alta Consulting to deliver effective and reliable regulatory guidance and creative solutions to address their unique needs. Services include regulatory submission, FDA cGMP compliance, QA, validations, and marketing entry services for our international clients. Our focus has been to provide effective solutions in an efficient manner. Click on the image below to learn about our workflow-based CAPA system.

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http://www.altaq.com/Validations.html

US Market entry support. Call us for a quote! Alta Consulting offers a full range of validation services to medical device, pharmaceutical, and biotechnology companies. Our experts assist our clients from validation planning through execution and final reporting. Alta Consulting can assist clients to achieve their goals, whether the project involves information systems, a single unit, or a complete facility. Filling and Packaging Equipment Qualification. Computer and Software Validation.

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http://www.altaq.com/index.html

US Market entry support. US Market entry support. Call us for a free quote! We provide global regulatory, compliance, and validation consulting services to the pharmaceutical, biologics, diagnostics, and medical device industries. We are an organization with a focus on customer needs and benefits. Alta Consulting believes in developing efficient and cost-effective regulatory solutions by understanding clients’ needs and applying best practices. 510(k), IDE, and PMA. IND, NDA, and BLA. 21 CFR Part 11.

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http://www.altaq.com/usdistribution.html

US Market entry support. US Market entry support. Click on the images below to download a brochure. The USA is one of the largest consumer and industrial markets in the world with a population of more than 300 million that accounts for more that 50% of the global medical device market. The USA also has a strong domestic medical device manufacturing sector and thousands of distributors that operate nationally, regionally, and locally. Review of Competing Medical and IVD Products. Where possible we work wi...

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US Market entry support. US Market entry support. Call us for a free quote! We provide global regulatory, compliance, and validation consulting services to the pharmaceutical, biologics, diagnostics, and medical device industries. We are an organization with a focus on customer needs and benefits. Alta Consulting believes in developing efficient and cost-effective regulatory solutions by understanding clients’ needs and applying best practices. 510(k), IDE, and PMA. IND, NDA, and BLA. 21 CFR Part 11.

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