Documents & Documentation
Quality
Responsibility
Definitions
Regulation
100

Written instructions designed to contain details on how to do a specific task correctly.

SOPs

100

A failure that is caught before and/or during the manufacture of product?

Deviation 

100

The person/people who are responsible for the facility, quality system, organizational structure and ensuring adequate resources.

Management

100

Under the law, if a company is not complying with cGMP regulations, any drug it makes is considered ______.

Adulterated

100

How often, as a minimum, are GMP facilities inspected by the FDA?

2 years

200

Records used to demonstrate compliance with internal policies, procedures, and regulatory requirements

GMP Documents

200

What do GMPs ensure?

Drug products are safe, pure and effective.

200

Department responsible for approval or rejection of components, raw materials, containers, closures etc.

Quality

200

SUB

Single Use Bioreactor

200

The minimum and most recent requirements that must be followed to assure that the products are safe, pure, effective and of the highest quality.

cGMPs

300

Finish the phrase: “If it isn’t documented,…”

it didn’t happen”

300

_______ cannot be tested into a batch of product but must be built into each batch of product during all stages of the manufacturing process.

Quality

300

The health protection agency that regulates the pharmaceutical industry is

FDA

300

The 5 cGMP characteristics of a drug are

Purity, Safety, Quality, Strength and Identity

300

It critically important to follow GMP regulation because

It’s the LAW.

400

These types of documents are legal documents and can be subpoenaed in a court of law as evidence.

GMP Records

400

Which group performs in lab testing of product quality?

Quality Control Group (QC)

400

The person/people who are responsible for product safety, quality and effectiveness.

Everyone

400

cGMPs

Current Good Manufacturing Practices

400

The consumer health protection agency that regulates the pharmaceutical industry.

FDA

500

These types of practices are used to ensure proper documentation is adhered to when documenting manufacturing related activities.

GDPs- Good documentation practices 

500

A failure that is caught after the release of manufactured product to the market

Recall

500

The person/people most responsible for personnel accountability.

Yourself 

500

ALCOA

Attributable, Legible, Contemporaneous, Original, Accurate

500

Pharmaceutical regulations across the world play an important role in ensuring the ______ and _______ of the approved drugs.

safety & efficacy