Build Your Qualification Package

Tell us what your Quality Unit needs. We’ll organize the request and connect you directly with the right people.

Approximately 3 minutes

Tell us about your organization

This helps us prepare the right qualification information the first time.

Name *

Work Email *

Company *

Job Title

Phone

Organization Type *

Primary Testing Need

Target Qualification Date

Choose the documents you need

Select everything required for your supplier qualification file.

Documents RequestedW-9Quality Self-AssessmentOrganizational ChartCertificate of InsuranceQuality AgreementAudit SchedulingTechnical Capability InformationNDA or Confidentiality AgreementOther Document

Audit PlumGXP

Tell us whether an audit is part of your qualification process.

Would you like to conduct an audit?YesNot at This TimeNot Sure—Please Advise

Preferred Audit TypeOnsite AuditVirtual AuditPaper or Document AuditOpen to the Most Appropriate Option

Preferred Audit Date

Audit Scope or Areas of Focus

Upload Your Qualification Documents

Send your supplier survey, NDA, audit agenda or other documents directly to the PlumGXP Quality team.

Upload DocumentsYou may upload multiple PDF, Word or Excel documents.

Drag and Drop (or) Choose Files

Anything Else Your Quality Team Needs?

Share any special requirements that will help us prepare your qualification package.

Additional Request

Quality Agreement or NDA PreferenceWe Will Provide Our DocumentPlease Provide PlumGXP’s DocumentNot RequiredTo Be Determined

Save as Draft

Please do not fill in this field.

YOUR QUALITY TEAM

Katie Neetz

Quality Director

Katie will review your requirements, coordinate qualification documents and follow up on open items.

Katie.Neetz@PlumGxP.com
610.800.0155

Supplier qualification support
Quality agreement coordination
Onsite, virtual and paper audits
Scientific and compliance questions

PlumGxP

Allentown, PA

A GxP pharmaceutical contract microbiological and analytical testing laboratory located in PA serving pharmaceutical, biotech, cell and gene therapy, and medical device organizations.

Confidence in Every Result

FDA Registered

ISO/IEC 17025 Planned Q4 2026

License to handle Schedule I to V Planned early Q4 2026