Frequently Asked Questions

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Investment varies based on product complexity, ingredient count, and regulatory requirements. Custom formulations typically range from [your range, e.g., $3,000-$8,000+], optimization projects from [$2,000-$5,000], and consultations from [$800-$2,000]. I provide transparent quotes after our discovery call once I understand your specific needs.

I require 50% deposit to begin work and 50% upon project completion and delivery of final documentation. For larger projects over [amount], payment plans can be arranged with milestone-based payments.Formulyn works with clients of all sizes, from small businesses to large corporations. We also work with non-profit organizations and government agencies.

Custom formulation development: 6-8 weeks. Formula optimization: 4-6 weeks. Expert consultations: 2-3 weeks. Timeline depends on project complexity and your responsiveness during the review stages. Rush services available for urgent projects.

For new formulations: your product concept, target benefits, intended audience, budget range, and timeline. For optimization: your current formula, specific challenges you're facing, and production details. For consultations: the specific technical question or formula you need reviewed. 

Absolutely! I work with brands globally and am experienced with TGA (Australia), FDA (USA), Health Canada, and EU regulatory frameworks. All communication happens via email and video calls, making location irrelevant.Rush services available for urgent projects.

Yes. I sign Non-Disclosure Agreements before any project discussion. All formulations and business information are kept strictly confidential.Rush services available for urgent projects.

You own it completely. Once final payment is made, all intellectual property rights transfer to you. I retain no ownership or rights to use your formula.

Absolutely. Professional ethics and legal agreements prevent me from sharing any client work. Each formula is custom and confidential to your brand only.

I hold an MS in Biochemistry (Gold Medalist) and have 5+ years of hands-on experience in pharmaceutical and nutraceutical R&D. I've worked as an R&D Manager and Quality Assurance Officer, managing GMP compliance, TGA standards, and developing formulations from concept through manufacturing.

My specialty areas include dietary supplements (capsules, tablets, powders, gummies), skincare and topical products, functional foods and beverages, and pet supplements. I work across various categories including vitamins, probiotics, adaptogens, nootropics, sports nutrition, and wellness blends

I've worked with a wide range of ingredients and categories. If you have something specific in mind, let's discuss it during our discovery call. If it's outside my expertise, I'll be upfront and can refer you to specialists in that area.

No, I'm a formulation consultant, not a manufacturer. However, I provide comprehensive documentation that any GMP-certified manufacturer can use. I can also recommend manufacturing partners suitable for your product and production scale.

Yes. Unlike theoretical formulators, I design formulations with real-world manufacturing in mind - considering equipment limitations, stability, cost, and scalability. My background includes working directly with manufacturers, so I know what works on the production floor.

Yes! I maintain relationships with reputable manufacturers in Australia and internationally. I can recommend partners based on your product type, batch size, budget, and location preferences.

All my projects include 30 days of post-delivery support for manufacturer technical questions at no additional cost. I'm available to clarify specifications, troubleshoot production issues, or make minor adjustments.

Yes. Regulatory compliance is built into every formula I develop. I ensure adherence to TGA (Australia), FDA (USA), and international standards including proper ingredient selection, dosage limits, and claims substantiation. However, final regulatory approval is your responsibility - I provide the compliant foundation.

I provide guidance on compliant claims based on your formula and can review label drafts for accuracy. For full label design and regulatory submissions, I can refer you to specialized regulatory consultants or work alongside your team.

I stay current with regulatory updates. If significant changes affect your formula within 6 months of delivery, I'll notify you and discuss necessary adjustments at a reduced rate

Moderately involved at key milestones. I'll need your input during the discovery phase, when reviewing the initial formula blueprint, and before finalization. Expect 3-4 check-ins throughout the project. I handle all the technical work - you make strategic decisions.

Primarily via email for updates and documentation, with video calls for discovery, midpoint review, and final handover. I respond to emails within 24 business hours and provide regular progress updates.

I include revision rounds in each package (typically 1-2, depending on the service). We'll work together until you're satisfied. If there's a fundamental misalignment, I'll work with you to find a solution. Client satisfaction is my priority.

Due to the custom nature of formulation work, deposits are non-refundable once work begins. However, if I cannot deliver the agreed-upon scope, I'll refund any unused portion. I've never had this situation because I'm very careful about setting clear expectations upfront.

Absolutely! Book a free 30-minute discovery call. We'll discuss your needs, and I'll recommend the best approach for your situation - no obligation.

Possibly! During our discovery call, we can discuss scaled options or phased approaches. I'm invested in helping great products come to life, and I'm open to creative solutions for the right projects.

Email me directly at  info@formulyn.com.au I typically respond within 24 hours and can schedule calls within the same week.