◎ Patent application
| Preliminary research and data preparation | Security testing | Data organization and writing | Application submission and official review |
3-6 months | 6-12 months (Some complex toxicology tests have a long cycle) | 1-2 months | 3-9 months (including data correction and communication feedback time) |
| Detection category | Core testing items | Difficulties and challenges |
|---|---|---|
| Physical and chemical properties | Characteristics, purity, stability, solubility, pH value, particle size distribution, etc | Difficulty in method developmentEspecially for natural extracts or synthetic polymers with complex structures. Stability dataIt is the basis for judging shelf life and usage safety, with strict conditions. |
| Microbial indicators | Total bacterial count, mold and yeast, heat-resistant Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, etc | Ensure that the raw materials themselves and during production and storage are not contaminated by microorganisms, and evaluateAnti corrosion challengeThe scheme design is complex. |
| Toxicological testing | (This is the most difficult and core part) • Basic three items: Skin irritant/corrosive, eye irritant, skin allergy • Advanced ProjectsGenetic toxicity (Ames, micronuclei, etc.), subchronic toxicity (28 day/90 day repeated dose), teratogenicity, toxicokinetics, etc | 1. High costThe cost of a complete set of toxicology tests can reach tens of thousands to millions. 2. Extremely long cycleThe 90 day repeated dose toxicity test itself requires nearly six months. 3. Strong strategic approachHow to determine based on raw material characteristics, exposure levels, etcDesign scientifically and reasonably; Toxicology Testing Strategy; It is the key to reducing costs and time, and it also tests the capabilities of service providers the most. |
| Functional basis | Provide experimental data or literature that proves the claimed efficacy of the raw materials. | Rigorous design is requiredIn vitro or human efficacy testingThe data must have statistical significance, and the report must comply with standards to avoid exaggerating promotional risks. |
| Patent type | Protection focus and applicable scenarios | Service Content |
|---|---|---|
| Invention Patent | ProtectionFormula, process, method, new useWaiting for core technology. • Composite patentProtect the specific composition and ratio of raw materials. • Method patentProtect the unique preparation process and extraction technology of raw materials. • Usage patentProtect raw materials from new and non obvious applications in cosmetics. | 1. Deep excavationCommunicate with your technical team to extract the most creative technical points. 2. Strategic layoutDetermine the optimal scope of protection and claims. 3. Document WritingWrite high-quality instructions and claims to ensure maximum protection. 4. Submission and ResponseSubmit the entire process on behalf of the agent and respond to the notice of review comments. |
| Utility model patent | Protecting productsSpecific structure and shapeWait. • Suitable for: raw materials with new microstructures (such as special crystal forms, capsule structures), innovative packaging containers, specialized production equipment, etc. | 1. Structural sortingHelp you clarify the structural innovation points that can be protected. 2. Drawing up blueprintsAssist in creating or standardizing drawings that meet the requirements. 3. Document WritingFocus on the practicality and novelty of the structure when writing. |
| Design Patent | Protecting productsVisual Aesthetics Design • Suitable for: special shapes of raw material particles, unique designs of packaging bottles, etc. | 1. Design confirmationAssist in selecting the most recognizable designs. 2. View specificationPrepare six views and a three-dimensional diagram that meet the requirements. 3. Application submissionQuickly submit and follow up on the process. |
| Collaboration mode | Core Content |
|---|---|
| New product and active ingredient research and development | Molecular design, process research, formula optimization, and natural substance extraction of active ingredients for specific needs |
| Industrial Technology Alliance and Tutoring | Provide one-stop services for manufacturers in the form of membership, including technical consultation, regulatory guidance, instrument usage, and talent cultivation |
| Comprehensive R&D and efficacy evaluation | Provide full process services from raw material development, formula research and development to comprehensive safety and efficacy evaluation |
| Open Innovation Challenge | Enterprises propose specific technical challenges and solicit innovative solutions from research teams and startups in society |
| Main modules | Specific content | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Policy interpretation and application planningdiv class="custom-table-container"
| Analyze the reward policies and key support directions of various provinces and cities (such as the transformation of scientific and technological achievements), and plan the most suitable application award types, nomination channels, and application paths based on the actual situation of enterprises | ||||||||||||
Planning and Writing of Core Technology Materialsdiv class="custom-table-container"
| Extracting innovative '; Invention Point "; Or "; Innovation Point ";; Write a high-quality nomination letter, including project introduction, main technical content, etc; Guide the preparation of supporting materials for technological innovation | ||||||||||||
Nomination and Publicity Process Assistancediv class="custom-table-container"
| Assist in connecting with eligible nominating units (such as the municipal science and technology bureau, qualified societies) or nominating experts; Guide the disclosure process of internal requirements for all completion units and the units where the completion personnel are located to complete the project | ||||||||||||
Formal review and progress managementdiv class="custom-table-container"
| Review all application materials to ensure compliance with formal review requirements; Manage the entire declaration process and track key time nodes |