Ultimo aggiornamento: agosto 17, 2026

GOOD LABORATORY PRACTICE

training

Descrizione

Argomenti:

GLP Scope.

Definitions.

Applicability to studies performed under grants and contracts.

Inspection of a testing facility.

Personale.

Testing facility management.

Study director.

Quality assurance unit.

General.

Animal care facilities.

Animal supply facilities.

Facilities for handling test and control articles.

Laboratory operation areas.

Specimen and data storage facilities.

Equipment design.

Maintenance and calibration of equipment.

Standard operating procedures.

Reagents and solutions.

Test and control article characterization.

Test and control article handling.

Mixtures of articles with carriers.

Protocol.

Conduct of clinical and nonclinical laboratory study.

Reporting of clinical and nonclinical laboratory study results.

Storage and retrieval of records and data.

Retention of records.

Purpose.

Grounds for disqualification.

Notice of and opportunity for hearing on proposed

disqualification.

Final order on disqualification.

Actions upon disqualification.

Public disclosure of information regarding disqualification.

For more details please send us e-mail: [email protected]

Speaking Opportunities

Our conference programmes are painstakingly researched over a period of months, ensuring that the agendas are always leading-edge, covering only those issues that matter to the marketplace. The speaker faculty is populated by individuals and organisations recommended to us by the market as leaders in their field.

Speaking at an NBScience event presents a unique platform from which to showcase the expertise of a high-profile representative from your organisation.

Speaking Can Involve:

A speaking slot on the conference agenda – a powerful platform from which to showcase the medical industry and knowledge and abilities of an expert in your organisation
Chairmanship of a conference session – a great way of aligning yourself with a high profile panel of medical industry experts
Involvement in an medical industry panel discussion as a panellist or chairperson – a chance to engage in industry-critical debate with market leading executives
Leading a one-day workshop before or after the medical conferencea more in-depth opportunity of demonstrating your expertise to a smaller, more focused group of individuals with specific needs and problems
To learn more about the benefits of speaking, and how to become more involved, please email: [email protected]

nbscience

Contatta NBScience

Dipartimento Educazione/Conferenze:

[email protected]

farmacologia

Revisione scientifica di casi

Revisione scientifica del caso

Ti piacerebbe capire se i programmi clinici sono attuali, recenti sviluppi della ricerca, o potrebbero esserlo gli approcci emergenti rilevante per la tua situazione individuale?

Condividi la tua domanda con il nostro team di ricerca scientifica e ricevi informazioni focalizzate sulle aree di ricerca attuale che potrebbero essere pertinente al tuo caso.

  • Revisione delle informazioni fornite
  • Informazioni rilevanti sulla ricerca e sul programma clinico
  • Una risposta chiara focalizzata sulla tua situazione
Cosa succede dopo? Invia la tua domanda, ricevere una revisione scientifica mirata, e ottieni una risposta chiara sulla ricerca e sui programmi clinici rilevanti per la tua situazione.
La tua revisione scientifica sarà preparata da Dott. Helen Melnik, Dottorato di ricerca , chi ha più di 25 anni di esperienza nella ricerca sulle cellule staminali e nei programmi clinici internazionali.

Nessun obbligo. La tua domanda verrà esaminata in modo confidenziale.

Solo informazioni didattiche e di ricerca. Questo servizio no costituiscono un parere medico, diagnosi, prescrizione, o uno personalizzato raccomandazione terapeutica.


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organizzazione di ricerca a contratto

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