|
Section 207.3
|
Establishment registration and product listing for human blood and blood products and for medical devices |
|
Section 207.7
|
Exemptions for establishments |
|
Section 207.10
|
Who must register and submit a drug list |
|
Section 207.20
|
Times for registration and drug listing |
|
Section 207.21
|
How and where to register and list drugs |
|
Section 207.22
|
Information required in registration and drug listing |
|
Section 207.25
|
Amendments to registration |
|
Section 207.26
|
Updating drug listing information |
|
Section 207.30
|
Additional drug listing information |
|
Section 207.31
|
Notification of registrant; drug establishment registration number and drug listing number |
|
Section 207.35
|
Inspection of registrations and drug listings |
|
Section 207.37
|
Misbranding by reference to registration or to registration number |
|
Section 207.39
|
Establishment registration and drug listing requirements for foreign establishments |
|
Section 207.40
|
Scope and purpose |