RQM+ Emails and Contacts
RQM+ is one of the leading Other Companies in United States Of America having its headquarters at Monroeville, Pennsylvania . RQM+ has a large market share in Regulatory for Medical Device , Quality Systems for Medical Device , Design Assurance for Medical Device , Product Quality for Medical Device , Post-Market Surveillance for Medical Device , EU MDR , Clinical Evaluation Reports , Remediation , Form 483, Warning Letter, Consent Decree , Complaint Remediation , Manufacturing Site Transfer , 510(k), PMA, De Novo , UDI Compliance , Supplier Quality , Process Validation , Human Factors , Design Verification and Validation , Design History File Remediation , Design Quality Assurance , FDA Mock Audit , In Vitro Diagnostics products and services. As it is a Privately Held Company so there are 251 - 500 employees working in RQM+. Even RQM+ generates a yearly revenue of 251 - 500 every year making it one of the top players in the Other industry. This company has 251 - 500 employees, and you can see the emails and phone numbers of the top 10 working professionals in RQM+.
- View Emails/Numbers
- Monroeville, Pennsylvania
Detailed Overview of RQM+ | Emails & Phone
Company Name
RQM+
Official Contact
******3182
Official Address
2790 Mosside Blvd. ,Suite 800, Monroeville, Pennsy... More
Industry Type
Other
Employees Range
251 - 500
Revenue Range
251 - 500
Company Type
Privately Held
Official Website
https://www.rqmplus.com/
Products/Services
Regulatory for Medical Device , Quality Systems fo... More
RQM+ - Designation, Email Address and Phone Numbers
Check the Email and Phone Number List of the Top Management working at the RQM+
| Name | Designation | Email Address | Contact Number | View Email & Phone |
|---|---|---|---|---|
| ***ris Lee*** | Director, Business Development | ****@rqmplus.com | ******4925 | View Email & Phone |
| ***ria Fag*** | President | ****@rqmplus.com | ******2421 | View Email & Phone |
| ***ven Don*** | Project Controller | ****@rqmplus.com | ******8833 | View Email & Phone |
| ***oel Kee*** | Sr. Director, Data Operations | ****@rqmplus.com | ******7542 | View Email & Phone |
| ***rie Dem*** | Director of Human Resources | ****@rqmplus.com | ******8106 | View Email & Phone |
| ***ndy Loc*** | Program Manager | ****@rqmplus.com | ******1395 | View Email & Phone |
| ***rew Lak*** | Senior Consultant | ****@rqmplus.com | ******5703 | View Email & Phone |
| ***vid Osb*** | Consultant | ****@rqmplus.com | ******6718 | View Email & Phone |
| ***ina Pha*** | Senior Regulatory Consultant | ****@rqmplus.com | ******2447 | View Email & Phone |
| ***hel Low*** | Consultant | ****@rqmplus.com | ******3977 | View Email & Phone |
How do Emails and Phone Numbers of RQM+ Help in Bringing Leads?
After viewing all the RQM+ employees' emails like the emails of the CXO, Sales Head, Management, CFO Contact, Marketing Head, Managing Director,Founder, HR Head Email, Admin, O Level, CEO, and other Key Employees you can use the Connect+ Email Marketing Tool to send them bulk emails and generate leads. RQM+ has a revenue of 251 - 500 and 251 - 500 employees are working at Dabur to whom you can hit the emails.
Companies Similar to
RQM+
Here are some companies that are similar to RQM+ as all of them are from the Other industry.
All of these companies operate in Regulatory for Medical Device , Quality Systems for Medical Device , Design Assurance for Medical Device , Product Quality for Medical Device , Post-Market Surveillance for Medical Device , EU MDR , Clinical Evaluation Reports , Remediation , Form 483, Warning Letter, Consent Decree , Complaint Remediation , Manufacturing Site Transfer , 510(k), PMA, De Novo , UDI Compliance , Supplier Quality , Process Validation , Human Factors , Design Verification and Validation , Design History File Remediation , Design Quality Assurance , FDA Mock Audit , In Vitro Diagnostics and you can pick any of them and get an Overview with their employee’s email address as they are similar to RQM+.
| Name | Industry | Headquarters | No. of Employees |
|---|---|---|---|
| Arconic | Other | Delhi,India | 51 - 100 |
| SCA - Hygiene and Forest Products Company | Other | Maharashtra,India | 51 - 100 |
| Keystone Technologies | Other | Pennsylvania,United States Of America | 101 - 250 |
| Premier Dental Products Company/USA | Other | Pennsylvania,United States Of America | 101 - 250 |
| Xodus Medical | Other | Pennsylvania,United States Of America | 51 - 100 |
| Name | Industry | Headquarters | No. of Employees |
|---|---|---|---|
| Teoxane Laboratories | Other | 251 - 500 | |
| Zahrawi Group | Other | 251 - 500 | |
| Spectrum Plastics Group | Other | Georgia,United States Of America | 251 - 500 |
| AccuMED Corp. | Other | North Carolina,United States Of America | 251 - 500 |
| Hamilton Medical | Other | Graubünden,Switzerland | 251 - 500 |
Key Competitors of RQM+
You should not miss the competitors of RQM+ because you can even target RQM+’s competitors to promote your product through email marketing. Their Product and Services might differ from RQM+ but the employee size they all have is 251 - 500 employees.
Frequently Asked Questions
Where is the Headquarters of RQM+?
The headquarters of RQM+ is in Pennsylvania, United States Of America
What is the Official Website of the RQM+?
The Official Website of the RQM+ is https://www.rqmplus.com/
What is the industry type of RQM+?
The Industry type of RQM+ is Other
How many employees are there at RQM+?
The overall employees at RQM+ are 251 - 500
What is the yearly Revenue generated every month by RQM+?
RQM+ generates an income of 251 - 500 in a year
What are the Products and Services offered by RQM+?
The products and services offered by RQM+ are Regulatory for Medical Device , Quality Systems for Medical Device , Design Assurance for Medical Device , Product Quality for Medical Device , Post-Market Surveillance for Medical Device , EU MDR , Clinical Evaluation Reports , Remediation , Form 483, Warning Letter, Consent Decree , Complaint Remediation , Manufacturing Site Transfer , 510(k), PMA, De Novo , UDI Compliance , Supplier Quality , Process Validation , Human Factors , Design Verification and Validation , Design History File Remediation , Design Quality Assurance , FDA Mock Audit , In Vitro Diagnostics
Disclaimer: We incorporate several data points to give structure, flow, and efficacy to the information provided, and we use the best and most reliable sources (primary and secondary research, public information).
- © 2024 SalezShark.com. All rights reserved.
