№ files_lp_4_process_1_51868
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This document outlines the validated method for cannabinoid testing, specifically targeting CBD, THC, and related substances in MCT oil formulations.
Year: 2026
Region / City: In-house
Subject: Cannabinoid Assay in MCT Oil
Document Type: Method Validation Report
Organization / Institution: Pharmalytics
Author: In-house
Target Audience: Analysts and Supervisors
Period of Validity: N/A
Approval Date: N/A
Date of Changes: N/A
Price: 8 / 10 USD
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Cannabinoid Quantification in Cannabis Flowers - Method Validation for Dried Basis Analysis
Note: Year
CLP classification and labelling of formulations containing micro-encapsulated chemicals
Year: 2024
Place: Brussels
Document reference: Doc. CA/12/2023 rev. 2
Meeting: 52nd Meeting of Competent Authorities for REACH and CLP (CARACAL)
Session: Open session
Meeting dates: 1–2 July 2024
Meeting format: Hybrid
Concern: CLP classification and labelling of formulations containing micro-encapsulated chemicals
Agenda point: CLP Open session, AP 7
Action requested: Discussion and comments
Deadline for written comments: 4 September 2024
Issuing bodies: European Commission Directorate-General for Environment; Directorate-General for Internal Market, Industry, Entrepreneurship and SMEs
Regulatory framework: CLP Regulation; REACH Regulation
Document status: Revision 2
Revision history: Simplification following comments from AT, NL, SE and CropLife Europe
Purpose: Collection of CARACAL views on classification and labelling approaches
Target group: Competent authorities under REACH and CLP
AI Technical Specifications and Testing Methodologies for Formulations
Year: 19xx
Note: Region / City
Subject: Chemical testing methods for AI formulations
Document Type: Technical specification
Target Audience: Technical specialists in chemical analysis and formulation
Supplementary Information for Performance of vicinal diols ethoxylate containing double hydrophilic headgroups in metal cleaner formulations
Year: Not specified
Region / City: Taiyuan, Shanxi, China
Theme: Surfactant properties, metal cleaning
Document Type: Research article
Organization / Institution: College of Chemistry and Chemical Engineering, Shanxi Key Laboratory of Chemical Product Engineering, Taiyuan University of Technology
Author: Jing Huang, Qingwen Dong, Xu Li, Lei Liu, Jinxiang Dong
Target Audience: Researchers, chemical engineers, surfactant formulators
Effective Period: Not specified
Approval Date: Not specified
Date of Changes: Not specified
Increasing the lung dose of inhaled suspensions – Comparison between microsuspension and nanosuspension formulations delivered by a breath-actuated mesh nebuliser
Year: 2026
Region / city: Taipei City, Helsinki, Malmö
Topic: Pharmaceutical formulation, Inhalation therapy
Document type: Research article
Institution: HCmed Innovations Co. Ltd., Nanoform Finland Oyj, Inhaled Delivery Consulting AB
Author: Edgar H. Cuevas Brun, Barry Derham, Yulia Degtyareva, Pablo Luis Gutierrez Carvalho, Gunilla Petersson, Sarah Byrne, Lucy Hardaker, Jesse Heikkilä, Elisabetta Micelotta
Target audience: Researchers, pharmaceutical professionals, healthcare practitioners
Period of validity: N/A
Date of approval: N/A
Date of changes: N/A
Lipid nanoparticle formulations for in vitro transfection of Jurkat cells
Year: 2026
Region / City: Not specified
Subject: Lipid nanoparticles, gene delivery, T cell transfection
Document type: Research supplementary material
Institution: Not specified
Author: Not specified
Target audience: Researchers in molecular biology and gene therapy
Experimental system: Jurkat cells
Analyzed molecules: DOPE, Cholesterol, C12-200, C14-PEG 2000, CAR-CD19BBz, ZsGreen pDNA
Methods: Microfluidic mixing, electroporation, Lipofectamine comparison
Measured parameters: Hydrodynamic diameter, polydispersity index, zeta potential, cell viability, transfection efficiency
Figures included: S1–S5
Statistical analysis: One-way ANOVA, unpaired t test
Supporting Information File 1: Methods and Model Formulations for Estimating No-Effect Toxicity Concentrations in Ecotoxicology Simulation Studies
Field: Ecotoxicology
Document type: Supporting information file
Content type: Methodological appendix with model formulations and simulation data
Subject: Estimation of no-effect toxicity concentrations (NEC) and ECx metrics
Models described: NEC3param, NEC4param, ECxLinear, ECxExp, ECxSigmoidal, ECx4param, ECxWeibull1, ECxWeibull2
Software / framework: jagsNEC (Bayesian modelling approach)
Key parameters: τ (upper plateau / intercept), η (NEC), β (decay rate), δ (lower plateau), ω (EC50)
Methods included: Threshold models, sigmoidal decay models, Weibull models
Data type: Simulated toxicity and concentration–response data
Simulation design: Multiple sampling schemes with varying treatment levels, replicates, and binomial trials
Measured variable: Concentration–response relationships for toxicity effects
Chemical context: Weathered Ichthys condensate WAF expressed as Total Aromatic Hydrocarbons (µg/L TAH)
Biological context: Tropical marine species responses including A. millepora, S. variolaris, N. dorsatus, and A. amphitrite
Statistical approach: Bayesian model fitting with MCMC and DIC-based model weighting
Included materials: R functions for simulation data generation, model equations, simulation study tables, and figure of fitted concentration–response curves
Tables: Model weight comparison (Table S1); toxicity estimates and effects across simulation designs (Table S2)
Figure: Concentration–response relationships with Bayesian NEC-sigmoidal model fits (Figure S1)
Physicochemical quality indicators of liquid toilet soap formulations with IGFE
Year: 2026
Region / city: Not specified
Theme: Physicochemical properties of liquid soap
Document type: Research study
Author: Not specified
Target audience: Researchers, chemists, professionals in the cosmetics industry
Period of validity: Not applicable
Approval date: Not specified
Modification date: Not specified
ULTRA LOW VOLUME LIQUID FORMULATIONS: SPECIFICATIONS AND TESTING REQUIREMENTS
Year: Not specified
Region / Organization: FAO/WHO
Subject: Agrochemical formulation standards
Document type: Technical guideline
Active ingredient: Defined per ISO common name
Form: Homogeneous liquid
Storage conditions: 0 ± 2 °C for 7 days, 54 ± 2 °C for 14 days
Viscosity: As specified in MT 22.1
Impurities: By-products of manufacture or storage, water content limits
Testing methods: CIPAC, AOAC or equivalent
Purpose: Establish parameters for UL formulation stability, identity, and drift potential
Publication reference: CIPAC number / UL (month & year of publication)
Topics: MCT Cannabinoid formulations