Non-Disclosure Agreement — Physical Development Services — Sweet Little Crumb

Legal Document

Non-Disclosure Agreement

Physical Development Services

Custom Formulation Development, Reformulation Development, Reverse Engineering, Stability Testing, Project Management, and Lab Batch Production

Cosmetic formulation laboratory

Section 1

Parties and Recitals

Recitals

WHEREAS, the Consultant provides specialised cosmetic product development and reformulation services, including custom formulation development, reverse engineering, manufacturing process development, stability testing, project management, and lab batch production services;

WHEREAS, the Client desires to engage the Consultant’s services for product development, physical reformulation, or related physical cosmetic science services;

WHEREAS, during the course of the engagement, both parties will exchange highly sensitive and proprietary information including product concepts, formulation data, physical samples, manufacturing processes, supplier relationships, business strategies, market intelligence, and technical methodologies;

WHEREAS, the protection of confidential information is critical to both parties’ commercial success and competitive advantage in the global cosmetics industry;

NOW THEREFORE, in consideration of the mutual covenants and agreements contained herein, and for other good and valuable consideration (the receipt and sufficiency of which are hereby acknowledged), the parties agree as follows:

Section 2

Definitions

“Confidential Information”

Means any and all non-public, proprietary, or confidential information disclosed by either party to the other, whether orally, in writing, electronically, visually, or in any other form, including but not limited to:

  • Cosmetic and personal care product formulations, including ingredient lists, percentages, processing methods, and technical specifications
  • Physical samples, prototypes, and benchmark products provided for analysis
  • Manufacturing processes, procedures, techniques, scale-up parameters, and know-how
  • Intellectual property, trade secrets, proprietary methodologies, and technical data
  • Supplier relationships, ingredient sourcing information, and pricing structures
  • Stability testing data, preservative efficacy results, and performance data
  • Customer lists, business relationships, and distribution strategies
  • Regulatory compliance strategies, testing protocols, and safety assessments
  • Market research, competitive analyses, business plans, and strategic information
  • Financial information, cost structures, and commercial terms
  • Research and development data, experimental results, and laboratory findings
  • and any information marked, designated, or reasonably understood to be confidential.

“Permitted Purpose”

Means the legitimate business purpose for which Confidential Information is disclosed, specifically relating to the provision or receipt of physical cosmetic product development services.

“Disclosing Party”

Means the party disclosing Confidential Information.

“Receiving Party”

Means the party receiving Confidential Information.

Cosmetic formulation

Section 3

Confidentiality Obligations

3.1

Non-Disclosure

The Receiving Party agrees to hold all Confidential Information in strict confidence and shall not disclose, reveal, or make available such information to any third party without the prior written consent of the Disclosing Party.

3.2

Non-Use

The Receiving Party shall not use Confidential Information for any purpose other than the Permitted Purpose and shall not use such information for its own benefit or the benefit of any third party.

3.3

Standard of Care

The Receiving Party shall exercise the same degree of care to protect Confidential Information as it exercises to protect its own confidential information of a similar nature, but in no event less than reasonable care.

3.4

Need-to-Know Basis

The Receiving Party may disclose Confidential Information only to its employees, consultants, advisors, or agents who (a) have a legitimate need to know such information for the Permitted Purpose, (b) have been informed of the confidential nature of such information, and (c) are bound by confidentiality obligations at least as restrictive as those contained herein.

Section 4

Exceptions to Confidentiality

The obligations set forth in Section 3 shall not apply to information that:

4.1 Public Domain

Is or becomes generally available to the public through no breach of this Agreement by the Receiving Party.

4.2 Prior Knowledge

Was known to the Receiving Party prior to disclosure, as evidenced by written records predating such disclosure.

4.3 Independent Development

Is independently developed by the Receiving Party without use of or reference to the Confidential Information, as evidenced by written records.

4.4 Third Party Disclosure

Is rightfully received by the Receiving Party from a third party without breach of any confidentiality obligation.

4.5 Required Disclosure

Is required to be disclosed by law, regulation, court order, or governmental authority, provided that the Receiving Party gives the Disclosing Party reasonable advance notice (where legally permissible) to enable the Disclosing Party to seek protective measures.

Laboratory work

Section 5

Intellectual Property Rights

5.1.1. Each party retains all rights, title, and interest in and to its pre-existing intellectual property. Nothing in this Agreement grants any licence or right to the intellectual property of either party except as expressly set forth herein.

5.2 Client Formulations

5.2.1. Upon full payment of all agreed fees, the Client receives complete ownership of the final approved formulation, including the formula, manufacturing method, and associated documentation.
5.2.2. The Consultant retains ownership of all preliminary work, development concepts, trial formulations, and unapproved formulations generated during the development process. These remain the Consultant’s intellectual property.

5.3 Developed IP

5.3.1. Any intellectual property developed jointly during the engagement shall be owned as specified in the separate Services Agreement between the parties. In the absence of such specification, joint developments shall be owned proportionally based on each party’s contribution.

5.4 Consultant’s General Knowledge

5.4.1. The Consultant retains ownership of all general techniques, knowledge, methodologies, scientific principles, manufacturing approaches, and professional skills utilised or further developed during the engagement.
5.4.2. The Consultant will not replicate the Client’s exact formulation for other clients. However, the Consultant may apply general knowledge, techniques, and manufacturing insights gained during the engagement to future projects, provided no Confidential Information is disclosed.

5.5 Benchmark Products

5.5.1. Where the Client provides benchmark products for reverse engineering, the Consultant’s analysis and interpretation of such products remains the Consultant’s intellectual property. The resulting formulation developed for the Client becomes the Client’s property upon full payment.

5.6 Research and Educational Use

5.6.1. The Consultant may retain anonymised data for research, quality improvement, regulatory compliance tracking, and educational purposes, provided no Client-identifying or formulation-identifying information is disclosed.
Cosmetic ingredients

Section 6

Regulatory Compliance

6.1

Australian Compliance

Both parties acknowledge their obligations under Australian law, including but not limited to the Privacy Act 1988 (Cth), Competition and Consumer Act 2010 (Cth), Therapeutic Goods Act 1989 (Cth), and applicable state legislation.

6.2

International Compliance

For worldwide services, both parties shall comply with applicable international regulations, including but not limited to European Union Cosmetics Regulation, United States FDA regulations, Health Canada regulations, and other applicable jurisdiction-specific requirements.

6.3

AICIS Compliance

The Consultant maintains compliance with the Australian Industrial Chemicals Introduction Scheme (AICIS) and shall ensure all recommendations comply with current Australian chemical regulatory requirements.

Section 7

Data Protection and Privacy

7.1. Both parties shall handle any personal information in accordance with the Privacy Act 1988 (Cth) and the Australian Privacy Principles.
7.2. Both parties shall implement appropriate technical and organisational measures to protect Confidential Information against unauthorised access, disclosure, alteration, or destruction.
7.3. Any cross-border transfer of personal information shall comply with applicable privacy laws and regulations.
7.4. The Consultant’s full Privacy Policy is available as a separate document and forms part of the engagement terms.

Section 8

Return of Materials

8.1. Upon termination of this Agreement or upon written request by the Disclosing Party, the Receiving Party shall promptly return or destroy (at the Disclosing Party’s option) all documents, materials, and other tangible items containing or representing Confidential Information, together with all copies thereof in any form.
8.2. The Receiving Party shall provide written confirmation of destruction where requested.
Cosmetic science

Section 9

Term and Termination

Sign
Agreement commences
5 yr
Active term of Agreement
+10 yr
Confidentiality obligations survive
30 d
Cure period for breach
9.1. Term. This Agreement shall commence on the date last signed below and shall remain in effect for a period of five (5) years, unless earlier terminated in accordance with this Agreement.
9.2. Survival. The obligations of confidentiality set forth herein shall survive termination of this Agreement and shall continue for a period of ten (10) years following such termination.
9.3. Termination for Breach. Either party may terminate this Agreement immediately upon written notice if the other party materially breaches this Agreement and fails to cure such breach within thirty (30) days after receiving written notice thereof.

Section 10

Remedies

10.1

Equitable Relief

The Receiving Party acknowledges that disclosure of Confidential Information would cause irreparable harm to the Disclosing Party for which monetary damages would be inadequate. Therefore, the Disclosing Party shall be entitled to seek equitable relief, including injunction and specific performance, without prejudice to any other rights or remedies.

10.2

Monetary Damages

In addition to equitable relief, the Disclosing Party may seek monetary damages, including actual damages suffered, profits gained by the Receiving Party from unauthorised use or disclosure, and legal costs and expenses incurred in enforcing this Agreement.

10.3

Liquidated Damages

For breach of confidentiality obligations, the Receiving Party shall pay liquidated damages of AUD $5,000 per incident, which the parties agree represents a reasonable estimate of the harm likely to result from such breach.

Formulation work

Section 11

Governing Law and Jurisdiction

11.1. This Agreement shall be governed by and construed in accordance with the laws of Queensland, Australia, without regard to conflict of law principles.
11.2. The parties hereby submit to the exclusive jurisdiction of the courts of Queensland, Australia.
11.3. Before initiating court proceedings, the parties agree to attempt to resolve any disputes through good faith negotiations for a period of thirty (30) days. If such negotiations fail, the parties may agree to mediation under the Australian Commercial Disputes Centre rules.

Section 12

General Provisions

12.1 Entire Agreement

This Agreement constitutes the entire agreement between the parties with respect to confidentiality and supersedes all prior agreements, understandings, and communications on this subject, whether written or oral.

12.2 Amendment

This Agreement may be amended only by a written instrument signed by both parties.

12.3 Severability

If any provision is held to be invalid or unenforceable, the remaining provisions shall continue in full force and effect.

12.4 Waiver

No waiver of any provision shall be deemed or shall constitute a waiver of any other provision.

12.5 Assignment

Neither party may assign this Agreement without the prior written consent of the other party.

12.6 Counterparts

This Agreement may be executed in counterparts (including electronic counterparts), each of which shall be deemed an original.

12.7 Electronic Signatures

The parties agree that electronic signatures shall have the same legal effect as handwritten signatures.

Skincare products

Acknowledgement

Signatures

By signing below, the parties acknowledge that they have read, understood, and agree to be bound by the terms and conditions of this Agreement. This Agreement has been prepared in accordance with Australian law and international best practices for cosmetic science consultancy services. Legal advice should be sought before execution.

Consultant Signature

Sweet Little Crumb / This Formulating Life

Name
Natalie Skiller
Consultant
Date
25/03/2026
Date signed
Signature
Consultant signature
Witness Signature
Witness signature
Witness Name
Glen Skiller
Witness
Witness Date
25/03/2026
Date witnessed

Client Signature

Client Name / Company Name
 
Date
 
Client Signature (or typed full legal name)
 
Client Address
 
Client Email
 
Client Phone
 
Witness Name
 
Witness Date