This document provides an overview of Scale-Up and Post-Approval Changes (SUPAC) guidelines. It defines SUPAC and the scientific rationale for the guidelines, which aim to expedite post-approval changes while ensuring safety and effectiveness. The FDA has issued SUPAC guidelines for immediate-release, modified-release, and semi-solid dosage forms. These guidelines provide recommendations for post-approval changes to components/composition, manufacturing sites, batch size (scale-up), and manufacturing processes/equipment. They define three levels of changes and specify the tests, documentation, and required filings for each level. The document reviews the SUPAC guidelines sections in detail and discusses limitations of the current guidelines.
DRUG MASTER FILE
Presented by :
RUSHIKESH D MENDHE
Roll no - 511
Mpharm Ist Year
(Department of Pharmaceutics)
Content : :
INTRODUCTION
TYPES OF DMF
DMF FORMAT & ASSEMBLY
DELIVERY OF DMF TO FDA
SUBMISSION OF DMF
THE MECHANISM OF A DRUG MASTER FILE
CTD & ELECTRONIC DMFS
UPDATES TO DMF
CLOSURE OF A DRUG MASTER FILE
APPLICATION OF DMF
REFERENCE
INTRODUCTION :
A Drug Master File (DMF) is a submission to the Food and Drug Administration (FDA) that may be used to provide confidential detailed information about facilities, processes, or articles used in the manufacturing, processing, packaging, and storing of one or more human drugs.
This guideline does not impose mandatory requirements.
Objectives :
Main Objective of the DMF is to support regulatory requirements
To prove the quality, safety and efficacy of the medicinal product
TYPES OF DMF :
DMF FORMAT & ASSEMBLY :
The DMF is submitted as Original and Duplicate jackets, collated, assembled, paginated, and jacketed, using covers obtained from the government printing office and a respecifically provided for the DMFs
Multiple volumes are numbered, and the paper must be standard paper size
Paper length should not be less than 10 inches nor more than 12 inches.
Each volume of a DMF should be not more than 2 inches thick
DELIVERY OF DMF TO FDA :
DMF should be submitted at following address :
Food and Drug Administration Center for Drug Evaluation and Research Central Document Room 5901 – B Ammendale Road Beltsville, MARYLAND 20705-1266 USA
SUBMISSION OF DMF :
The DMF must be submitted in two copies, one with a blue cover and one with a red cover.
Each page of each copy of the DMF should be dated and consecutively numbered.
Each DMF submission should contain :
• A Transmittal letter
• Administrative information about the submission
• Other specific information
A. Transmittal Letter :
i) Original Submissions :
• Identification of submission: Original, the type of DMF as classified in Section III, and its subject.
• Identification of the applications, if known, that the DMF is intended to support, including the name and address of each sponsor, applicant, or holder, and all relevant document numbers.
• Signature of the holder or the authorized representative.
• Typewritten name and title of the signer.
ii) Ammendments :
• Identification of submission: Amendment, the DMF number, type of DMF, and the subject of the amendment.
• A description of the purpose of submission, e.g., update, revised formula, or revised process.
• Signature of the holder or the authorized representative.
• Typewritten name and title of the signer.
B. Administrative information about the submission:
DRUG MASTER FILE
Presented by :
RUSHIKESH D MENDHE
Roll no - 511
Mpharm Ist Year
(Department of Pharmaceutics)
Content : :
INTRODUCTION
TYPES OF DMF
DMF FORMAT & ASSEMBLY
DELIVERY OF DMF TO FDA
SUBMISSION OF DMF
THE MECHANISM OF A DRUG MASTER FILE
CTD & ELECTRONIC DMFS
UPDATES TO DMF
CLOSURE OF A DRUG MASTER FILE
APPLICATION OF DMF
REFERENCE
INTRODUCTION :
A Drug Master File (DMF) is a submission to the Food and Drug Administration (FDA) that may be used to provide confidential detailed information about facilities, processes, or articles used in the manufacturing, processing, packaging, and storing of one or more human drugs.
This guideline does not impose mandatory requirements.
Objectives :
Main Objective of the DMF is to support regulatory requirements
To prove the quality, safety and efficacy of the medicinal product
TYPES OF DMF :
DMF FORMAT & ASSEMBLY :
The DMF is submitted as Original and Duplicate jackets, collated, assembled, paginated, and jacketed, using covers obtained from the government printing office and a respecifically provided for the DMFs
Multiple volumes are numbered, and the paper must be standard paper size
Paper length should not be less than 10 inches nor more than 12 inches.
Each volume of a DMF should be not more than 2 inches thick
DELIVERY OF DMF TO FDA :
DMF should be submitted at following address :
Food and Drug Administration Center for Drug Evaluation and Research Central Document Room 5901 – B Ammendale Road Beltsville, MARYLAND 20705-1266 USA
SUBMISSION OF DMF :
The DMF must be submitted in two copies, one with a blue cover and one with a red cover.
Each page of each copy of the DMF should be dated and consecutively numbered.
Each DMF submission should contain :
• A Transmittal letter
• Administrative information about the submission
• Other specific information
A. Transmittal Letter :
i) Original Submissions :
• Identification of submission: Original, the type of DMF as classified in Section III, and its subject.
• Identification of the applications, if known, that the DMF is intended to support, including the name and address of each sponsor, applicant, or holder, and all relevant document numbers.
• Signature of the holder or the authorized representative.
• Typewritten name and title of the signer.
ii) Ammendments :
• Identification of submission: Amendment, the DMF number, type of DMF, and the subject of the amendment.
• A description of the purpose of submission, e.g., update, revised formula, or revised process.
• Signature of the holder or the authorized representative.
• Typewritten name and title of the signer.
B. Administrative information about the submission:
Investigational medical product dossierSachinFartade
Investigational medical product dossier is document made to apply for clinical trial application in European Union. European Medical Agency is regulatory body for drug approval in European Union.
ATUL CHAUDHARY (STUDENTS)
DEPARTMENT OF PHARMACEUTICS
ISF COLLEGE OF PHARMACY, GHALKALAN, MOGA , PUNJAB
THIS SLIDE IS THE BEST SLIDE FOR PREPARING THE TOPIC SUPAC OF REGULATORY AFFAIRS SUBJECT
SLIDE ARE SPECIALLY DESIGN FOR MASTER STUDENTS AS WELL AS GRADUATION STUDENTS
The presentation is about: Drug Regulatory Affairs as a profession, Scope & Responsibilities in life cycle management of a drug and role of RA in the drug approval process.
COPP/CPP it certification of pharmaceutical product for reviewing QSE i.e. Quality, Sefty,Efficacy of product. it important certification for exporting it may required by importing country.
A brief presentation on the Code of Federal Regulations
Covers the following aspects -
- What is CFR?
-History of CFR
- CFR Title 21
- CFR in modern times.
- Research tools in CFR
Investigational medical product dossierSachinFartade
Investigational medical product dossier is document made to apply for clinical trial application in European Union. European Medical Agency is regulatory body for drug approval in European Union.
ATUL CHAUDHARY (STUDENTS)
DEPARTMENT OF PHARMACEUTICS
ISF COLLEGE OF PHARMACY, GHALKALAN, MOGA , PUNJAB
THIS SLIDE IS THE BEST SLIDE FOR PREPARING THE TOPIC SUPAC OF REGULATORY AFFAIRS SUBJECT
SLIDE ARE SPECIALLY DESIGN FOR MASTER STUDENTS AS WELL AS GRADUATION STUDENTS
The presentation is about: Drug Regulatory Affairs as a profession, Scope & Responsibilities in life cycle management of a drug and role of RA in the drug approval process.
COPP/CPP it certification of pharmaceutical product for reviewing QSE i.e. Quality, Sefty,Efficacy of product. it important certification for exporting it may required by importing country.
A brief presentation on the Code of Federal Regulations
Covers the following aspects -
- What is CFR?
-History of CFR
- CFR Title 21
- CFR in modern times.
- Research tools in CFR
Introduction to Scale up and post approval changes.
SUPAC Guidelines :
1.In component and composition
2.The site of manufacture
3.The scale up batch of manufacture
4.The manufacturing( equipment and process)
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http://sandymillin.wordpress.com/iateflwebinar2024
Published classroom materials form the basis of syllabuses, drive teacher professional development, and have a potentially huge influence on learners, teachers and education systems. All teachers also create their own materials, whether a few sentences on a blackboard, a highly-structured fully-realised online course, or anything in between. Despite this, the knowledge and skills needed to create effective language learning materials are rarely part of teacher training, and are mostly learnt by trial and error.
Knowledge and skills frameworks, generally called competency frameworks, for ELT teachers, trainers and managers have existed for a few years now. However, until I created one for my MA dissertation, there wasn’t one drawing together what we need to know and do to be able to effectively produce language learning materials.
This webinar will introduce you to my framework, highlighting the key competencies I identified from my research. It will also show how anybody involved in language teaching (any language, not just English!), teacher training, managing schools or developing language learning materials can benefit from using the framework.
Acetabularia Information For Class 9 .docxvaibhavrinwa19
Acetabularia acetabulum is a single-celled green alga that in its vegetative state is morphologically differentiated into a basal rhizoid and an axially elongated stalk, which bears whorls of branching hairs. The single diploid nucleus resides in the rhizoid.
1. Scale - Up and Post
Approval Changes
SUPAC
Presented By-
ROHIT
M.Pharmacy
(Pharmaceutics)1
2. Index
Definition
Scientific Rational
SUPAC Guidelines – SUPAC IR, SUPAC – MR,
SUPAC –SS
Levels of Change
Components and composition
Manufacturing Site Changes
Batch size change (Scale up)
Manufacturing change : Process & Equipment
Limitations of SUPAC
2
3. New Drug
Application (NDA)
approved by FDA
SCALE-UP Larger Batch size
Generic
Drug
Product
Bioequivalent to
the FDA
reference listed
drug
(RLD)product
ANDA
approved by
FDA
SCALE
UP
Larger Batch
size
3
4. What is SUPAC
In the process of developing a new drug product, the
batch sizes used in the earliest human studies are
small.
The size of the batches is gradually increased (Scale
- up).
The scale-up process and the changes made after
approval in the composition, manufacturing process,
manufacturing equipment, and change of site have
become known as Scale-Up and Post approval
Changes, or SUPAC.
4
5. Scientific Rationale
to expedite the processes of post approval
changes of drug products
FDA can assure their safety and effectiveness.
lower the regulatory burden for industry.
5
6. The FDA has issued various guidances for
SUPAC changes designated as
A.SUPAC-IR (for immediate-release solid oral
dosage forms),
B.SUPAC-MR (for modified-release solid oral
dosage forms), and
C.SUPAC-SS (for non-sterile semisolid dosage
forms including creams, ointments, gels, and
lotions).
6
7. Level of
Changes
• Minor change
• Moderate change
• Major change
• Application / Compendial Tests
• In Vitro Dissolution / Release
• In Vivo
• Annual Report
• Changes Being Effected
Supplement
• Prior Approval Supplement
Tests
Filing
SUPAC GUIDELINES -
DEFINE
7
8. Level 1: unlikely to have detectable
impact
Level 2: could have significant impact
Level 3: likely to have significant
impact
Levels of change
Likelihood of impact on formulation
quality and performance
8
9. These guidelines provide recommendations
for post approval changes in
(1) the components or composition,
(2) the site of manufacture,
(3) the scale-up of manufacture, and
(4) the manufacturing (process and equipment)
9
10. Components & Composition
This section focuses on changes in excipients in
the drug product
SUPAC-MR: Excipient critical or non critical to the
drug release.
- Changes in non release controlling excipients
- Changes in release controlling excipients
SUPAC-SS: Changes in preservative
10
11. SUPAC - IR
LEVE
L
CLASSIFICATI
ON
EXCIPIENT
RANGES
(%w/w of total
formulation)
TEST
DOCUMENTATIO
N
FILING
DOCUMENTA
TION
1
I
-Delition or Filler -stability •Annual
partial delition ±5 -application/ report
of an Disintegrant compendial
ingredient Starch requirements
(colour, flavor ±3
or change in Other
ingredient of ±1
the ink) Binder
-Changes in ±0.5
excipients, Lubricant
expressed as Calcium (Ca) or
% (w/w) of Magnesium (Mg)
total Stearate
formulation, ±0.25
less than or Other
equal to ±1
1
12. LEVE
L
CLASSIFICA
TION
EXCIPIENT
RANGES
(%w/w of total
formulation)
TEST
DOCUMENTATION
FILING
DOCUMEN
TATION
-change in Filler -stability •Prior
technical ±10 application/compendial approval
grade of Disintegrant requirements suppleme
excipients Starch -Dissolution data nt
-Changes in ±6 depends on solubility, •Annual
excipients, Other ±1 theraputic range and report
expressed Binder permeability.
as % (w/w) ±1 Case A : High
of total Lubricant Permeability, High
formulation, Calcium (Ca) or Solubility Drugs
greater than Magnesium (Mg) Single point
II Level 1 Stearate Dissolution profile .
changes. ±0.5 Case B : Low
Other Permeability, High
±2 Solubility Drugs
Glidant Multi point dissolution
Talc profile
12
±2
Other
Case C :High
Permeability, Low
±0.2 Solubility Drugs
13. LEVEL CLASSIFICATION TEST
DOCUMENTATION
FILING
DOCUMENTATIO
N
-Higher than
SUPAC-IR Level 1
and Level 2
excipient ranges.
-stability
application/compendial
requirements
•Prior approval
supplement
•Annual report
III
-Case B dissolution
profile (Multi-point
dissolution profile in
the application
/compendial medium at
15, 30, 45, 60, and 120
minutes or until an
asymptote is reached
for the proposed and
currently accepted
formulation.)
-Biostudy or IVIVC
13
14. SUPAC – MR Non Release Controlling
LEVE
L
CLASSIFICATION ExcipTiEeSnTDtsOCUMENTATION FILING
I
-Delition or partial delition
of an ingredient
-upto SUPAC-IR Level 1
excipient ranges
-stability
-application/compendial
requirements
•Annual
report
II
-change in technical grade
of excipients
-upto SUPAC-IR Level 2
excipient ranges
-stability
application/compendial
requirements
-Multi-point dissolution
profiles (15,30,45,60 & 120
min)
USP buffer media at pH 4.5-
7.5 for extended release)
Three different Media (e.g.,
Water, 0.1N HCl, and USP
buffer media at Ph 4.5 And
6.8 for delayed release)
•Prior
approval
supplemen
t
•Annual
report
14
III
-Higher than SUPAC-IR
Level 1 and Level 2
excipient ranges.
-stability
application/compendial
requirements
-Biostudy or IVIVC
•Prior
approval
supplemen
15. SUPAC – MR Release Controlling
LEVE
L
CLASSIFICATION ExTEcSiTpDiOeCnUMtsENTATION FILING
DOCUMEN-
TATION
I
-≤ 5% w/w
change based on
total release
controlling
excipient
content.
-No other
changes
-stability
-application/compendial
requirements
•Annual
report
II
15
-change in
technical grade
of excipients
-≤ 10% w/w
change based on
total release
controlling
excipient
content.
-stability
application/compendial
requirements
-Multi-point dissolution profiles
(15,30,45,60 & 120 min)
USP buffer pH 4.5-7.5 for extended
release) Three different Media (e.g.,
Water, 0.1N HCl, and USP buffer
media at Ph 4.5 And 6.8 for DR
release)
•Prior
approval
supplement
•Annual
report
16. SUPAC – SS Components and Composition
LEVE
L
CLASSIFICATION TEST DOCUMENTATION FILING
I
-Delition or partial delition of
an ingredient
-change in supplier or
technical grade of any other
excipient
-Upto 5 % change in approved
amount of ingredient.
-stability
-application/ compendial
requirements
•Annual
report
II
-Upto >5 % and ≤ 10 % change
in approved amount of
ingredient.
-Change in particle size
distribution of the drug
substance, if the drug is in
Suspension
-change in supplier or
technical grade of any other
excipient
-stability
application/compendial
requirements
-in vitro release test
•Changes
being
effected
suppleme
nt
•Annual
report
16
-change in approved amount
of ingredient.
-Change in crystalline form of
-stability
application/compendial
•Prior
approval
17. SUPAC – SS Components and Composition -
LEVE
L
CLASSIFICATION
PrT
eES
sT
eD
rvO
aCU
tiM
vE
eNTATION FILING
I
Quantitatively
10% or less
change in the
approved amount
of preservative
-application/compendial
requirements
-Preservative effectiveness test
at lowest specified preservative
level
•Annual report
II
10% -20 % change
in the approved
amount of
preservative
-application/compendial
requirements
-Preservative effectiveness test
at lowest specified preservative
level
•Changes
being effected
supplement
•Annual report
III
7
> 20% change in
the approved
amount of
preservative
(including
deletion) or use of
a different
preservative.
-application/compendial
requirements
-executed batch records
-For new preservative:
analytical method for
identification and assay;
validation studies
-Preservative effectiveness test
at lowest specified preservative
•Prior approval
supplement
•Annual report
1
18. Manufacturing Site Changes
changes in location of the site of manufacture,
packaging operations and/or analytical testing
laboratory
do not include any scale-up changes, changes in
manufacturing (including process and/or
equipment), or changes in components or
composition.
current Good Manufacturing Practice (CGMP)
inspection.
18
19. LEVEL CLASSIFICATION TEST DOCUMENTATION FILING
DOCUMENTATI
-ON
I
-Site change
within a single
facility
-No change in
SOP,
environmental
conditions or
equipments used
-Common
personnels
application/compendi
al requirements
•Annual
report
19
20. LEVE
L
CLASSIFICATIO
N
TEST DOCUMENTATION FILING
II
-Same
continuous
campus
-Common
personnel
-No other
changes
-application/compendial
requirements
-Notification of Location of new
site
-Updated batch records
SUPAC – MR
-Multi-point dissolution profiles
(15,30,45,60 & 120 min)
USP buffer media at pH 4.5-7.5 for
extended release) Three different
Media (e.g., Water, 0.1N HCl, and
USP buffer media at Ph 4.5 And 6.8
for delayed release)until 80% of
Drug Released.
•Annual report
•Changes
being Effected
Supplement
20
21. LEVE
L
CLASSIFICATIO
N
TEST DOCUMENTATION FILING
-Different
campus
-Different
personnel
-application/compendial
requirements
-Notification of Location of new
site
-Updated batch record
Annual report
Prior approval
supplement
III
SUPAC –IR
Multi-point dissolution profile in
the application/compendial
medium
21
SUPAC – MR
-Multi-point dissolution profiles
(15,30,45,60 & 120 min)
USP buffer media at pH 4.5-7.5 for
extended release) Three different
Media (e.g., Water, 0.1N HCl, and
USP buffer media at Ph 4.5 And 6.8
for delayed release) untill 80 % of
22. Batch Size Change (Scale Up)
changes in the size of a batch from the pivotal/pilot
scale biobatch material to larger production batches
compliance with CGMP's
No change in SOP, formulation and manufacturing
procedures or equipments used
All scale-up changes should be properly validated
the minimum batch size for the pivotal clinical trial
batch or biobatch be at least 100000 dosage units
/100 kg or 10% of a production batch, whichever is
larger.
22
23. LEVE
L
CLASSIFICATI
ON
TEST DOCUMENTATION FILING
I Change in
batch size, up
to and
including a
factor of 10
times the size
of the
pilot/biobatch
Updated batch records
application/compendial
requirements
stability
•Annual
report
II Changes in
batch size
beyond a factor
of ten times the
size of the pilot
or biobatch,
No other
changes
-Updated batch records
-application/compendial
requirements
-Stability
SUPAC –IR
Multi-point dissolution profiles
SUPAC – MR
-Multi-point dissolution profiles in
multiple medias (e.g., USP buffer
media at pH 4.5-7.5 for extended
release) three other media (e.g.,
Water, 0.1N HCl, and USP buffer
media at Ph 4.5 And 6.8 for delayed
•Annual
report
•Changes
being
Effected
Suppleme
nt
23
24. Manufacturing Changes
Changes affecting:
- Equipments
- Manufacturing process
Appropriate validation studies are conducted
24
25. Equipments
LEVE
L
CLASSIFICATION TEST DOCUMENTATION FILING
I
-Alternate equipment
of same design and
principles
Automated
equipments
-Updated batch records
-application/compendial
requirements
stability
•Annual
report
II
25
Change to equipment
of different design and
principle
Updated batch records
application/compendial
requirements
Stability
SUPAC –IR
Multi-point dissolution
profiles in multiple
medias
SUPAC – MR
-Multi-point dissolution
profiles in multiple
medias
•Annual
report
•Changes
being
Effected
Supplement
26. Manufacturing Changes-
Process
LEVE
L
CLASSIFICATION TEST DOCUMENTATION FILING
I -Adjustment of
equipment
operating
conditions
(operating
speeds, mixing
times)
-Updated batch records
-application/compendial
requirements
-stability
•Annual
report
Within approved
application ranges
26
27. LEVE
L
CLASSIFICATI
ON
TEST DOCUMENTATION FILING
-Adjustment of
equipment
operating
conditions
(operating
speeds, mixing
times)
-Updated batch records
-application/compendial
requirements
-Stability
SUPAC-IR
Multi-point dissolution profile
•Annual
report
•Changes
being
Effected
Suppleme
nt
II
Beyond
approved
application
ranges
-SUPAC – SS
Change in the
process of
combining two
phases
SUPAC-MR
-Multi-point dissolution profiles in
multiple medias (e.g., USP buffer
media at pH 4.5-7.5 for extended
release) three other media (e.g.,
Water, 0.1N HCl, and USP buffer
media at Ph 4.5 And 6.8 for delayed
release)
SUPAC-SS
In vitro release test Documentation27
28. LEVEL CLASSIFICATI
ON
TEST DOCUMENTATION FILING
III
(SUPAC-IR
SUPAC-
MR)
Changes in the
type of process
used (e.g. wet
granulation to
direct
compression
-Updated batch records
-application/compendial
requirements
-Stability
-Biostudy or IVIVC
•Prior
approval
suppleme
nt
•Annual
report
SUPAC-IR
Multi-point dissolution profile
SUPAC-MR
Multi-point dissolution profiles
in multiple medias (e.g., USP
buffer media at pH 4.5-7.5 for
extended release) three other
media (e.g., Water, 0.1N HCl,
and USP buffer media at Ph 4.5
And 6.8 for delayed release)
28
29. Using
Similarity Factor, f2
FDA has placed more emphasis on a dissolution
profile comparison in the area of post-approval
changes
Among several methods investigated for
dissolution profile comparison, f2 is the
simplest.
f2 = 50 + log {[1+ (1/n) ∑t=1 * n (Rt-Tt)2]-0.5 *100}
(where Rt and Tt are the cumulative percentage
dissolved at each of the selected n time points
of the reference and test product respectively.
When the two profiles are identical, f2=100. FDA
has set a public standard of f2 value between 50-
100 to indicate similarity between two
dissolution profiles.
29
30. SUPAC limitations
SUPAC:
► has not been updated (1995/97 for main guides)
► does not discuss multiple changes
► does not cover modified equipment
► must be used in conjunction with
other references, e.g. excipient handbook
30