Research + Development + innovation

Moehs has opted for a corporate R&D center to support all the factories of the Group and all our customers .     In this way, resources are optimized and a high knowledge of the products and processes is guaranteed from the beginning of their study in the laboratory until their commercialization.

The main objective of the R&D Department is the incorporation of new products to its line of development with the aim of diversifying the portfolio of the Moehs group. Proper selection of new products and planning of development activities allow our customers to launch their generics early, thus increasing their added value.

Directing and managing the group’s activity is the Steering Committee that encourages the implementation of internal and external training programs in accordance with the strategic objectives of the Company and the specific needs related to work activity, with special emphasis on Good Manufacturing
Practices, Security and environment.

Stages of the new generic product

Custom product synthesis

The initial development of the synthesis of a new generic is based on the deep analysis of three critical aspects.As for Custom Manufacturing, the begining of development is defined.
The commercial interest of our clients.
The patent situation.
The feasibility of the different synthesis routes.
The valuation of the confidential information recieved by our clientes.
The adaptability of the process transferred to our facilities.

MARKET ASSESSMENT

EXTERNAL PROPOSAL

RESEARCH AND EVALUATION
VIABILITY
PATENT STATUS

TRANSFER OF "KNOW HOW"  
CONFIDENTIALITY AGREEMENT
LABORATORY STUDYSAFETY ASSESMENT     
IMPACT OF WASTE TREATMENT
INDUSTRIAL VIABILITY
SAFETY ASSESSMENT         
IMPACT OF WASTE TREATMENT
TERMS AND CONDITIONS OF THE TEST PRODUCTIONS
SUPPLY AGREEMENT
SYNTHESIS ROUTE
PILOT LOTS          
PREPARING THE DMF
SAMPLE OFFER
PRODUCT SCALINGPRODUCT SCALING
VALIDATION PROCESSVALIDATION PROCESS
INDUSTRIAL PRODUCTIONINDUSTRIAL PRODUCTION
OPTIMIZATIONOPTIMIZATION
El desarrollo inicial de la síntesis de un nuevo genérico se basa en el análisis profundo de tres aspectos críticos:
En cuanto a un Custom Manufacturing, el inicio del desarrollo lo definen:
El interés comercial de nuestros clientes. La situación de patentes. La viabilidad de las diferentes rutas de síntesis
La valoración de la información confidencial recibida por nuestros clientes. La adaptabilidad del proceso transferido a nuestras instalaciones.
EVALUACIÓN DEL MERCADO
PROPUESTA EXTERNA
INVESTIGACIÓN Y EVALUACIÓN
VIABILIDAD
SITUACIÓN DE PATENTE
TRANSFERENCIA DE ‘KNOW HOW’
ACUERDO DE CONFIDENCIALIDAD
ESTUDIO DE LABORATORIO
EVALUACIÓN DE LA SEGURIDAD IMPACTO DEL TRATAMIENTO DE RESIDUOS VIABILIDAD INDUSTRIAL
EVALUACIÓN DE LA SEGURIDAD
IMPACTO DEL TRATAMIENTO DE RESIDUOS
RUTA DE SÍNTESIS
TÉRMINOS Y CONDICIONES
ACUERDO DE SUMINISTRO DE LA PRODUCCIÓN DE PRUEBA
LOTES PILOTO
PREPARACIÓN DEL DMF
OFERTA DE MUESTRA