Contact Us

GRP HeadQuaters USA

Boston

Address

550 Cochituate St, Framingham, East Wing, 4th floor, Suite 25, MA, 01701, USA

Telephone

Head Quarters: (+1) 781- 672-4200

Welcome!

Thank you for your interest in Global Regulatory Partners. Please fill out this short survey to help us better understand your needs.

All questions on this survey are general questions and are not brand specific.

Information of this survey will be used to connect you to the correct team member and enable our team to create customized proposals for your project

Requesting Company Information (Required)

Name of the Company(Required)

Field of Interest(Required)

Website Link(Required)

Industry Type(Required)

Number of Employees(Required)

Number of products on the market(Required)

Address(Required)

Street Address City State / Province / Region ZIP / Postal Code Country

Contact Details (Required)

Name(Required)

First Last

Phone(Required)

Email(Required)

Role

Department

Please choose country you are interested in(Required)

check all that apply

Australia

Brazil

Canada

China

European Union

Japan

Mexico

Multi-Country

United States of America

South Korea

Other-Not listened

Check the types of products you would like to register(Required)

check all that apply

Eye products ( ie. eyeshadow, mascara)

General Cosmetics (foundation, bronzer, blush)

Skin Care ( Facial cream, facewash, eye cream)

Acne Products ( Products with active ingredients used for acne)

Sunscreen

Insect repellent

Hair products ( shampoo, conditioners, hair masks)

Other

Other Product Type (please specify)(Required)

Is your cosmetic registered in any of the following countries?(Required)

check all that apply

USA

Australia

Canada

Brazil

Mexico

South Korea

Japan

China

Other

Other Country of Registration (please specify)(Required)

Approximately how many products would you like to register?(Required)

1-10

10-20

20-50

50-100

100+

What are your estimated Timelines for Company Market Access?(Required)

Urgent <2 months

2-5 months

6-12 months

13-24 months

Not decided

Is the Manufacturer of the cosmetics is located in what country?(Required)

check all that apply

USA

Australia

Canada

Brazil

Mexico

South Korea

Japan

China

Other

Other location country of the Manufacturer (please specify)(Required)

Is the cosmetic registered in the origin country (Manufacturer of the cosmetic)?(Required)

Yes

What Services are you interested in?(Required)

Regulatory Intelligence (report on regulatory process in the country)

Gap analysis (labeling and ingredient composition assessment)

Product Registration

Local Representation (necessary If you don’t have a local subsidiary and/or proper license)

The whole package!

Please choose country you are interested in(Required)

check all that apply

Australia

Brazil

Canada

China

European Union

Japan

Mexico

Multi- Country

United States of America

South Korea

Other-Not listened

What type of facility would you like audited?(Required)

check all that apply

Medical Device Manufacturing site

Drug Manufacturing Site

Clinical Trial site

Laboratory

Human cell/ tissue-based products Manufacturing Site

Approximately how many Audits would you like to schedule?(Required)

1-5

5-10

10+

When do you need these audits to be scheduled?(Required)

Urgent <2 months

2-5 months

6-12 months

13-14 months

Not decided

What services are you interested in ?(Required)

check all that apply

Quality Audit ( ISO 13485)

Pre-Health Authority Inspection Compliance

Good Laboratory Practice (GLP)

Good Manufacturing Practice (GMP)

Good Clinical Practice(GCP)

Current Good Tissues Practice (cGTP)

Routine Inspection

For Cause Inspection

Pre-approval Inspection (PAI)

How would the audit be conducted?(Required)

Onsite

Remote

Please choose country you are interested in(Required)

check all that apply

Australia

Brazil

Canada

China

European Union

Japan

Mexico

Multi-Country

United States of America

South Korea

Other-Not listened

Check the types of devices you would like to register (according to country of origin):(Required)

check all that apply

In vitro diagnostic device

Medical Device

Combination ( drug and medical device)

Cosmetic Medical device

Orphan Medical Device

Other

Other Device Type (please specify)(Required)

Is your device registered in any of the following countries?(Required)

check all that apply

USA

Australia

Canada

Brazil

Mexico

South Korea

Japan

China

Other

Other Registered Country (please specify)(Required)

Approximately how many products would you like to register?(Required)

1-5

5-10

10+

What are your estimated Timelines for Company Market Access?(Required)

Urgent <2 months

2- 5 months

6- 12 months

13 - 24 months

Not decided

Is the device manufactured in multiple sites ?(Required)

Yes

Are all sites ISO certified?(Required)

Yes

Yes, but not all

What services are you interested in ?(Required)

check all that apply

Regulatory Intelligence (report on regulatory process in the country)

Regulatory Strategy (report on pathway and timelines on how to receive market access in the country) (product specific)

Preliminary Gap analysis (product classification)

Product Registration

License Transfer

Local Representation (necessary If you don’t have a local subsidiary and/or proper license)

Clinical Trials

The whole package!

Please choose country you are interested in(Required)

check all that apply

Australia

Brazil

Canada

China

European Union

Japan

Mexico

Multi-Country

United States of America

South Korea

Other-Not listened

Check the types of drugs you would like to register ( according to country of origin):(Required)

check all that apply

Generic/biosimilar

Biologic

Vaccine

Over the Counter (OTC)

Combination [quasi-drug]

Radiopharmaceutical

Other

Other drug Type (Please Specify)(Required)

Is your drug registered in any of the following countries?(Required)

check all that apply

USA

Australia

Canada

Brazil

Mexico

South Korea

Japan

China

Other

Other Registered Country (Please Specify)(Required)

What stage is the product currently in?(Required)

check all that apply

Product Development

Pre-Clinical Trial

Clinical Trial Phase 1

Clinical Trial Phase 2

Clinical Trial Phase 3&4

Product Registration

Post-Registration

Approximately how many products would you like to register?(Required)

1-5

5-10

10+

What are your estimated Timelines for Company Market Access?(Required)

Urgent <2 months

2-5 months

6-12 months

13-24 months

Not decided

Who Manufactures the product?(Required)

Our company manufactures the product

Our Company has third-party contracts with manufacturers

We don’t manufacture the product

Is the Drug manufactured in multiple sites ?(Required)

Yes

Are all sites GMP certified?(Required)

Yes

Yes, but not all

What services are you interested in ?(Required)

check all that apply

Regulatory Intelligence (report on regulatory process in the country)

Regulatory Strategy (report on pathway and timelines on how to receive market access in the country) (product specific)

Preliminary Gap analysis (product classification)

Product Registration

License Transfer

Local Representation (necessary If you don’t have a local subsidiary and/or proper license)

Clinical Trials

The whole package!

Please choose country you are interested in(Required)

check all that apply

Australia

Brazil

Canada

China

European Union

Japan

Mexico

Multi-Country

United States of America

South Korea

Other-Not listened

Check the types of products you would like to register:(Required)

check all that apply

Vitamins

Probiotic

Hormones (i.e. Melatonin)

Other

Other Product to Register (Please Specify)(Required)

Do the products have claims listed on the label?(Required)

Yes

Is your Food Supplement registered in any of the following countries?(Required)

check all that apply

USA

Australia

Canada

Brazil

Mexico

South Korea

Japan

China

Other

Other Already-Registered Country (Please Specify)(Required)

Approximately how many products would you like to register?(Required)

1-10

10-20

20-50

50+

What are your estimated Timelines for Company Market Access?(Required)

Urgent <2 months

2-5 months

6-12 months

13-24 months

Not decided

In what country is the manufacturer located?(Required)

check all that apply

USA

Australia

Canada

Brazil

Mexico

South Korea

Japan

China

Other

Other Manufacturer Country-of-Origin (Please Specify)(Required)

What services are you interested in ?(Required)

check all that apply

Regulatory Intelligence (report on regulatory process in the country)

Gap analysis (Ingredient and Label Assessment, product classification)

Ingredient composition assessment

Label Assessment (Assessment of label according to local Regulation)

Product Registration

Local Representation (necessary If you don’t have a local subsidiary and/or proper license)

The whole package!

Please choose country you are interested in(Required)

check all that apply

Australia

Brazil

Canada

China

European Union

Japan

Mexico

Multi-Country

United States of America

South Korea

Other- Not listened

Other country of interest (Please Specify)(Required)

Check the types of products you would like to register(Required)

check all that apply

New Chemical

Disinfectant

Biocide

Other

Other type of product (Please Specify)(Required)

Check the uses of the product(Required)

check all that apply

Agricultural

Forestry

Domestic

Gardening

Industrial

Miscellaneous

Do the products have claims listed on the label?(Required)

Yes

Is your pesticide registered in any of the following countries?(Required)

check all that apply

USA

Australia

Canada

Brazil

Mexico

South Korea

Japan

China

Other

Other registered country (Please Specify)(Required)

Approximately how many products would you like to register?(Required)

1-5

What are your estimated Timelines for Company Market Access?(Required)

Urgent <2 months

2-5 months

6-12 months

13- 24 months

Not decided

Is the Manufacturer of the supplement is located in what country?(Required)

check all that apply

USA

Australia

Canada

Brazil

Mexico

South Korea

Japan

China

Other

Other manufacturer country (Please Specify)(Required)

What services are you interested in ?(Required)

check all that apply

Regulatory Intelligence (report on regulatory process in the country)

Gap analysis (Ingredient and Label Assessment, product classification)

Ingredient composition assessment

Label Assessment (Assessment of label according to local Regulation)

Product Registration

Local Representation (necessary If you don’t have a local subsidiary and/or proper license)

The whole package!

Please choose country you are interested in(Required)

check all that apply

Australia

Brazil

Canada

China

European Union

Japan

Mexico

Multi-Country

United States of America

South Korea

Other-Not listened

Other country of interest (Please Specify)(Required)

Check the types of products you would like to register(Required)

check all that apply

Vitamins (multi- mono)

Probiotic

Animal Feed

Other

Other country of interest (Please Specify)(Required)

Do the products have claims listed on the label?(Required)

Yes

Is your pet supplement registered in any of the following countries?(Required)

check all that apply

Australia

Canada

Brazil

Mexico

South Korea

Japan

China

Other

Other already-registered country (Please Specify)(Required)

Approximately how many products would you like to register?(Required)

1-10

10-20

20-50

50+

What are your estimated Timelines for Company Market Access?(Required)

Urgent <2 months

2-5 months

6-12 months

13-24 months

Not decided

Is the Manufacturer of the supplement is located in what country?(Required)

check all that apply

USA

Australia

Canada

Brazil

Mexico

South Korea

Japan

China

Other

Other manufacturer country (Please Specify)(Required)

What services are you interested in ?(Required)

check all that apply

Regulatory Intelligence (report on regulatory process in the country)

Gap analysis (Ingredient and Label Assessment, product classification)

Ingredient composition assessment

Label Assessment (Assessment of label according to local Regulation)

Product Registration

Local Representation (necessary If you don’t have a local subsidiary and/or proper license)

The whole package!

Name

This field is for validation purposes and should be left unchanged.

GRP USA Brochure

GRP is a global consulting and market access firm Headquartered in Boston Massachusetts USA that provides Regulatory Affairs, Quality, Clinical and Safety services to pharmaceutical and medical device companies worldwide to register their product with the Food and Drug Administration (FDA) the local Health Authority (HA)

US Representative - US Agent for foreign companies

White Paper: US Agent

The FDA requires any foreign establishment to appoint a United States agent ( U.S. agent ) for that establishment.

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Contact Us

GRP HeadQuaters USA

Boston

Address

Telephone

Welcome!

Requesting Company Information (Required)

Contact Details (Required)

ABOUT GRP GROUP

Useful Links

GRP Headquarters (USA)

22 Boston Warf Road, Boston, MA, 02210, USA

Tel : (+1 ) 781 - 672 -4200

Info@globalregulatorypartners.com

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